CN1525249B - Polymerizable composition and lithographic printing plate precursor - Google Patents

Polymerizable composition and lithographic printing plate precursor Download PDF

Info

Publication number
CN1525249B
CN1525249B CN2004100070091A CN200410007009A CN1525249B CN 1525249 B CN1525249 B CN 1525249B CN 2004100070091 A CN2004100070091 A CN 2004100070091A CN 200410007009 A CN200410007009 A CN 200410007009A CN 1525249 B CN1525249 B CN 1525249B
Authority
CN
China
Prior art keywords
compound
group
alkyl
aryl
phenyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CN2004100070091A
Other languages
Chinese (zh)
Other versions
CN1525249A (en
Inventor
藤牧一广
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Corp
Original Assignee
Fujifilm Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fujifilm Corp filed Critical Fujifilm Corp
Publication of CN1525249A publication Critical patent/CN1525249A/en
Application granted granted Critical
Publication of CN1525249B publication Critical patent/CN1525249B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C08K5/175—Amines; Quaternary ammonium compounds containing COOH-groups; Esters or salts thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C1/00—Forme preparation
    • B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
    • B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/36—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using a polymeric layer, which may be particulate and which is deformed or structurally changed with modification of its' properties, e.g. of its' optical hydrophobic-hydrophilic, solubility or permeability properties
    • B41M5/368—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using a polymeric layer, which may be particulate and which is deformed or structurally changed with modification of its' properties, e.g. of its' optical hydrophobic-hydrophilic, solubility or permeability properties involving the creation of a soluble/insoluble or hydrophilic/hydrophobic permeability pattern; Peel development
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C1/00—Forme preparation
    • B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
    • B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
    • B41C1/1016—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials characterised by structural details, e.g. protective layers, backcoat layers or several imaging layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2201/00—Location, type or constituents of the non-imaging layers in lithographic printing formes
    • B41C2201/02—Cover layers; Protective layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2201/00—Location, type or constituents of the non-imaging layers in lithographic printing formes
    • B41C2201/04—Intermediate layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2201/00—Location, type or constituents of the non-imaging layers in lithographic printing formes
    • B41C2201/14—Location, type or constituents of the non-imaging layers in lithographic printing formes characterised by macromolecular organic compounds, e.g. binder, adhesives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/04—Negative working, i.e. the non-exposed (non-imaged) areas are removed
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/06—Developable by an alkaline solution
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/22—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation characterised by organic non-macromolecular additives, e.g. dyes, UV-absorbers, plasticisers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
    • B41C2210/00—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation
    • B41C2210/24—Preparation or type or constituents of the imaging layers, in relation to lithographic printing forme preparation characterised by a macromolecular compound or binder obtained by reactions involving carbon-to-carbon unsaturated bonds, e.g. acrylics, vinyl polymers
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/0275—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with dithiol or polysulfide compounds
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/031—Organic compounds not covered by group G03F7/029
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
    • Y10S430/1055—Radiation sensitive composition or product or process of making
    • Y10S430/114—Initiator containing
    • Y10S430/117—Free radical
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/145—Infrared

Landscapes

  • Chemical & Material Sciences (AREA)
  • Optics & Photonics (AREA)
  • Physics & Mathematics (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials For Photolithography (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
  • Polymerisation Methods In General (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

A polyaerizable composition comprising: (A) a compound which causes at least one of decarboxylation and dehydration by heat; (B) a radical initiator; (C) a compound having at least one ethylenically unsaturated bond; and (D) an infrared ray absorber.

Description

Polymerisable composition
Technical field
The present invention relates to polymerisable composition, said composition is used for the image recording material of three-dimensional prototype, holography, planographic printing plate material, color proof, photoresist, color filter etc., and printing ink, paint, bonding agent etc.Particularly, the present invention relates to be suitable as the recording materials of negative planographic printing plate precursor, use this negative planographic printing plate precursor, can enough infrared lasers carry out so-called direct plate-making from the digital signal of computing machine etc.
Background technology
Laser instrument development in recent years significantly.Particularly for can emission wavelength being 760～1, ultrared solid state laser of 200nm and semiconductor laser (can be called " infrared laser " later on), these small size laser instruments with high output have become and have been easy to obtain.Particularly in the lithography field, these infrared lasers are very useful as recording light source in the direct plate-making of directly making galley according to the numerical data of computing machine etc.After this, about the Lighographic printing plate precursor recording materials to multiple laser beam sensitivity, people have also carried out various researchs.Known has pair photosensitive wavelength of infrared laser sensitivity more than or equal to the positive-type recording materials (seeing USP 4,708,925) of 760nm and the negative type recording materials (seeing JP-A-8-276558) of acid catalyst crosslink type.
Can comprise usually by the negative type image recording material that infrared ray exposure is write down: absorb the infrared beam energy, convert it into the infrared absorbent of heat, the heat that utilization obtains from infrared absorbent produces the radical initiator of free radical, and be initiating agent and the polymerizable compound of polymerization with the free radical that produces, and adopt following logging mode: the recording layer of exposure region (image recording material) is because of polymerizable compound appearance and the polymerization reaction take place formation image that is cured.There is such problem in these negative type image recording materials, promptly with utilizing ultrared energy the positive-type image recording material of recording layer dissolving are compared, and the sensitivity of negative type image recording material is low.Therefore, need, promptly with the infrared ray exposure back negative type image recording material that solubleness reduces greatly in developer solution by a kind of like this infrared record light source is had the image recording material that highly sensitive polymerisable compound is formed.
As for the image recording material that helps to improve sensitivity, known has: contain and light or hot material with excellent reactive component, for example chemical amplifying type photochromics (seeing JP-A-11-65105), and the photochromics (seeing JP-A-2000-89455) that utilizes the effect of alkene formula unsaturated polymerizable compound.And about utilizing the photochromics of alkene formula unsaturated polymerizable compound effect, known have a following photochromics: the photochromics (seeing JP-A-2002-82429) that has added the reduced form adjuvant, add the photochromics (seeing JP-A-2002-90985) of two thio-compounds etc. and added the photochromics (seeing WO 00/48836) of polybasic carboxylic acid compound.But, but any requirement that does not still have to satisfy sensitivity in these photochromicss with practical application.
And also there are the relatively poor worry of storage stability in these recording materials, and the unwanted reaction that takes place when for example handling under white light or owing to the variation of environment temperature is perhaps owing to airborne oxygen produces the polymerization obstacle.
Summary of the invention
Summary of the invention
Consider the defective of top described prior art, made the present invention, an object of the present invention is to provide a kind of polymerisable compound that can be used as the image recording layer of negative planographic printing plate precursor, this image recording layer has excellent sensitivity and storage stability, and wherein foregoing polymerisable compound is as its recording layer.
Inventor of the present invention has carried out research extensively and profoundly.As a result of, as a first aspect of the present invention, find to reach aforementioned purpose by adding an a kind of component that causes the compound of decarboxylation and/or dehydrogenation as polymerisable compound by heating.In addition, find to achieve the above object, cause of the present invention finishing by adding a kind of special monocarboxylic acid compound as this compound or replace this compound.
Particularly, polymerisable compound of the present invention is characterised in that: comprise that (A) is a kind of to cause the compound of decarboxylation and/or dehydrogenation by heating, (B) radical initiator (C) contains the compound of at least one alkene formula unsaturated link and (D) infrared absorbent.
Here, preferably (A) is a kind of causes that by heating the compound of decarboxylation and/or dehydrogenation is the compound that a kind of temperature at 100 ℃ to 300 ℃ causes decarboxylation and/or dehydrogenation.Especially, an embodiment preferred is wherein by being caused that by heating decarboxylation and/or dehydrogenation, this compound have the structure that can form 4 to 6 yuan of lactonic rings, lactam nucleus or cyclic acid anhydrides in molecule.
Preferably (A) is a kind of causes that by heating the more particular embodiment of the compound of decarboxylation and/or dehydrogenation is a kind of compound that contains at least a group by following formula (I) expression:
Figure G2004100070091D00031
Wherein:
X represents to be selected from-O-,-S-,-SO 2-,-NH-,-N (R 3)-and-divalent linker of CO-,
R 3Expression hydrogen atom or monovalence substituting group,
R 1And R 2Represent hydrogen atom or monovalence substituting group independently of one another, precondition is: R 1And R 2, R 1And R 2In any one and R 3Can be combined together to form ring texture.
For (A) compound the most preferred embodiment, that can mention has: by the monocarboxylic acid compound of following formula (I-2) expression:
Wherein:
A represents aromatic radical or heterocyclic radical,
R 1And R 2Represent hydrogen atom or monovalence substituting group independently of one another, precondition is: R 1And R 2, R 1And R 2In any one and X 1, R 1And R 2In any one and A, perhaps A and X 1Can be combined together to form ring texture,
X 1Expression is selected from-O--S-,-SO 2-,-NH-,-N (R 3)-,-CH 2-,-CH (R 4)-and-C (R 4) (R 5)-divalent linker and
R 3, R 4And R 5Represent hydrogen atom or monovalence substituting group independently of one another.
Particularly, in the present invention, the X in the preferred formula noted earlier (I-2) 1Be to be selected from-NH-,-N (R 3)-,-CH 2-,-CH (R 4)-and-C (R 4) (R 5)-divalent linker, more preferably-NH-and-N (R 3)-, and most preferably being-N (R 3)-.
For by R 3The substituting group of expression preferably contains in its structure-CO at least 2-and-CON (R 8)-in those of one.Most preferred R 3Structure be by following formula (i) or (ii) the expression structure.Particularly, compare, more preferably contain the substituting group of the amide structure of (ii) representing by formula with the substituting group that contains the ester structure of representing by formula (i).In following formula, R 6, R 7And R 8Represent hydrogen atom or monovalence substituting group independently of one another, and Z represents the monovalence substituting group.R 8Can be combined together to form ring structure with Z:
Figure G2004100070091D00041
Polymerisable compound according to second aspect present invention is characterised in that: comprise (A-1) a kind of monocarboxylic acid compound by foregoing formula (I-2) expression, (B) radical initiator (C) contains the compound of at least one alkene formula unsaturated link and (D) infrared absorbent.
The Lighographic printing plate precursor of third aspect present invention is characterised in that: comprise and have recording layer carrier thereon, described recording layer comprises the polymerisable compound of first aspect, and the Lighographic printing plate precursor of fourth aspect present invention is characterised in that: comprise and have recording layer carrier thereon, described recording layer is included in the described polymerisable compound of second aspect.
In the polymerisable compound of the photosensitive layer that is used as the negative planographic printing plate precursor usually,, effectively reduce the acid number of binder polymer in order to be suppressed at the exposure area owing to the damage of developing and causing.But, reduce acid number and can cause such problem, promptly the alkali solubility of territory, non-exposed area (non-image areas in the lithographic plate) can descend.In contrast, be in the preferred high acid value composition in elimination for the territory, non-exposed area, when composition was formed lithographic plate, the image-region that solidify the exposure back was subjected to easily developing and damages, and causes the reduction of printability resistance.
Although the mechanism of action of the present invention is still unclear, but can think as follows: when in polymerisable compound, use (A) a kind of compound that causes decarboxylation and/or dehydrogenation by heating, (randomly, below be called compound (A)), compound (A) carries out decarboxylation and/or dehydrogenation by the heat of infrared laser exposure generation, thus, compare before with exposure, the polarity of exposure area can become more hydrophobic.Thereby, after exposure, during the development treatment of use alkaline aqueous solution etc., can prevent effectively that the exposure area is subjected to the infiltration of developing solution, so be not easy to damage image-region.Therefore, when said composition is used as the recording layer of Lighographic printing plate precursor, can provide galley with excellent in resistance printing.
And in the territory, non-exposed area, compound (A) has high-dissolvability in alkaline development solution etc., and has excellent development capability, and reason is the hydroxy-acid group that can carry out decarboxylation or dehydrogenation in a large number intrinsic in its structure, or hydroxyl.Therefore, when said composition is used as the recording layer of Lighographic printing plate precursor, the galley that can provide its non-image areas to be difficult to tarnish.
Use be by the monocarboxylic acid compound of formula (I-2) expression (below, can abbreviate " monocarboxylic acid compound " as) situation under, this compound is the preferred embodiment of foregoing compound (A), can think by this compound is joined in the polymerizable compound, it and infrared absorbent (D) interact when exposure, improve the decomposition rate of radical initiator (B) thus. and, can think that the polymerization that produces causes free radical or the aggregation growth free radical causes free radical chain to be transferred in the monocarboxylic acid compound, thereby quicken to contain alkene formula unsaturated link compound (C) (below, can suitably be called " polymerizable compound ") polyreaction. therefore, the polymerisable compound that contains the oriented this monocarboxylic acid compound that wherein adds has high sensitivity, and can consider to use polymerisable compound of the present invention to be improved as the Lighographic printing plate precursor of recording layer film strength for image-region, and have excellent printability resistance. should be noted that, there is no need this (A-1) monocarboxylic acid compound is limited to a kind of compound that is caused decarboxylation and/or dehydrogenation by heating. the compound even without this physical property also is considered to manifest effect of the present invention, reason is that foregoing character is as interacting and the chain transfer performance. below, title does not cause that the compound that comprises (A-1) of this decarboxylation etc. is compound (A) yet sometimes.
Generally speaking, recited abovely can interactional compound take place when improving sensitivity with infrared absorbent or radical initiator when adding, can produce the adverse effect of the storage stability decline that makes composition itself in this polymerisable compound.But, be a kind of suitable compounds according to compound of the present invention (A), up to it by heating and decomposition with till inducing reaction as decarboxylation.Especially, under the situation that adds the monocarboxylic acid compound, do not cause this adverse effect.In addition, effect having appearred: has improved the effect based on the storage stability of the script deficiency of the photochromics of free radical polymerization.Can consider that monocarboxylic acid compound of the present invention and radical initiator form complex, thus between the storage life of undressed raw material thermally-stabilised radical initiator.
Detailed Description Of The Invention
Polymerisable compound of the present invention is characterised in that: comprise that (A) is a kind of to cause the compound of decarboxylation and/or dehydrogenation by heating, (B) radical initiator (C) contains the compound of alkene formula unsaturated link and (D) infrared absorbent.In addition, polymerisable compound of the present invention can contain (E) and be used to binder polymer that improves membrane property etc.Below all cpds that can be used for polymerisable compound of the present invention will be described successively.
The compound of decarboxylation and/or dehydrogenation [(A) cause] by heating
Do not limit especially and used in the present inventionly cause the compound of decarboxylation and/or dehydrogenation, as long as it by heating, preferably under 100 ℃ to 300 ℃ temperature conditions, causes that decarboxylation and/or dehydrogenation get final product by heating.That is, operable is to contain at least one is caused the functional group of decarboxylation and/or dehydrogenation by heating compound.More specifically, that can mention has: under 100 ℃ to 300 ℃ temperature, by decarboxylation and/or dehydrogenation, have the compound of structure of the cyclic acid anhydride of the lactonic ring that can form 4 to 6 yuan, 4 to 6 yuan lactam nucleus or 4 to 6 yuan.
As an instantiation of this compound (A), that can mention has: the compound that contains at least a group by following formula (I) expression:
Figure G2004100070091D00061
In the described in front formula (I), X represents to be selected from-O-,-S-,-SO 2-,-NH-,-N (R 3)-and-divalent linker of CO-; R 3Expression hydrogen atom or monovalence substituting group; And R 1And R 2Represent hydrogen atom or monovalence substituting group independently of one another.Incidentally, R 1And R 2, R 1And R 2In any one and R 3Can be combined together to form ring texture. in explanation, will describe these substituting groups in detail by the compound of formula (I-2) expression for more preferred.
In the present invention, enumerated the instantiation (1) of the compound that can be preferably used as at least a group by foregoing formula (I) expression of containing of compound (A) to (72).But, the invention is not restricted to this.
Figure G2004100070091D00091
Then, below will illustrate according to the synthetic embodiment of the representativeness of compound of the present invention (A), but be to be understood that the present invention is not limited to these.
Synthesizing of＜compound (46) 〉
In one 200 milliliters eggplant type flask, add the 3-methyl hydroxybenzoate of 9.9g and the 2-methyl chloropropionate of 8.4g, then to the N that wherein adds 65ml, the N-dimethyl acetamide. then, potassium iodide to sal tartari that wherein adds 5.8g and 2.8g, then in 100 ℃ of heating. after the potpourri that is obtaining reacted 10 hours, the reaction mixture that obtains is joined in the water of 300ml, and ethyl acetate extraction with 300ml. in a vacuum organic solvent is distilled, obtain the residue of 14.5g. then, the residue that 7.2g is obtained joins in 100 milliliters the eggplant type flask, in base, adding the water of 8ml and the methyl alcohol of 8ml then. the potpourri that will arrive is cooled to 0 ℃. then, to the NaOH that wherein adds 2.4g, and at room temperature reacted 12 hours. the reaction mixture that obtains is joined in the water of 200ml, and, obtain the compound (46) of 5.0g with the product of hydrochloric acid adjusting pH to 2. filtering-depositing. by MMR spectrum, IR spectrum and mass spectrophotometry spectrum confirm that this compound that obtains is compound (46).
Cause the most preferred embodiment of the compound of decarboxylation and/or dehydrogenation for (A) is a kind of by heating, what can mention is: by the monocarboxylic acid compound of following formula (I-2) expression.Should be noted in the discussion above that in (A-1) carboxylic acid compound those that can be similar to that use do not cause this decarboxylation and/or dehydrogenation replace compound (A).
Wherein:
A represents aromatic radical or heterocyclic radical,
R 1And R 2Represent hydrogen atom or monovalence substituting group independently of one another, its with contain at least one R by the compound of the group of aforementioned formula (I) expression 1And R 2In monovalence substituting group synonym.Precondition is: R 1And R 2, R 1And R 2In any one and X 1, R 1And R 2In any one and A, perhaps A and X 1Can be combined together to form ring texture,
X 1Expression is selected from-O--S-,-SO 2-,-NH-,-N (R 3)-,-CH 2-,-CH (R 4)-and-C (R 4) (R 5)-divalent linker and
R 3, R 4And R 5Represent hydrogen atom or monovalence substituting group independently of one another.
Here, in the molecular formula (I-2), the example of the aromatic radical of A representative comprises: phenyl ring, the condensed ring that the unsaturated ring of condensed ring that two or three phenyl ring form and phenyl ring and 5-unit forms.Instantiation comprises: phenyl, naphthyl, anthryl, phenanthryl, indenyl, acenaphthenyl and fluorenyl.Wherein more preferably phenyl and naphthyl.
This aryl can also have substituting group.Contain the aryl that will describe after substituent aryl example comprises, these aryl have the substituting group of other monovalence nonmetallic atom group beyond the hydrogen atoms on one or more one-tenth ring carbon atoms.Additional disclosure once, the preferred substituents example of Jie Shaoing comprises alkyl herein, substituted alkyl, and describe after a while be listed as substituent group in the substituted alkyl.
The heterocyclic radical example of A representative comprises: pyrroles's cyclic group, furans cyclic group, thiophene cyclic group, indoles cyclic group, the coumarone cyclic group, benzothiophene cyclic group, pyrazoles cyclic group, isoxazole cyclic group, the isothiazole cyclic group, indazole cyclic group, benzoisoxazole cyclic group, benzisothiazole cyclic group, the imidazoles cyclic group, oxazole cyclic group, thiazole cyclic group, benzimidazole cyclic group; benzoxazole cyclic group, benzothiazole cyclic group, pyridine cyclic group, quinoline cyclic group, isoquinolyl, pyridazine cyclic group, pyrimidine cyclic group, pyrazine cyclic group, 2,3-benzodiazine, quinazoline cyclic group, the quinoxaline cyclic group, phenanthridines cyclic group, carbazole cyclic group, the purine cyclic group, pyrans cyclic group, piperidines cyclic group, the piperazine cyclic group, morpholine cyclic group, indoles cyclic group, the indolizine cyclic group, chromene cyclic group, cinnoline cyclic group, acridine cyclic group, phenothiazine cyclic group, tetrazolium cyclic group and triazine cyclic group.
Heterocyclic radical can also contain substituting group.That will describe after substituent example comprises has hydrogen atoms other monovalence nonmetallic atom group group in addition as substituent the sort of on one or more one-tenth ring carbon atoms of aryl.
Secondly, in formula (I) and the formula (I-2), R 1And R 2The substituent example of monovalence of representative comprises: halogen atom, the optional amino that replaces, alkoxy carbonyl group, hydroxyl, ether, mercapto, thioether group, silicyl, nitro, cyano group, the optional alkyl that replaces, the optional thiazolinyl that replaces, the optional alkynyl that replaces, optional aryl that replaces and the optional heterocyclic radical that replaces.
As for such alkyl, that can enumerate has linearity, branching or a cyclic alkyl that contains 1～20 carbon atom.Instantiation comprises: methyl, ethyl, propyl group, butyl, amyl group, hexyl, heptyl, octyl group, nonyl, decyl, undecyl, dodecyl, tridecyl, cetyl, octadecyl, eicosyl, isopropyl, isobutyl, sec-butyl, the tert-butyl group, isopentyl, neopentyl, 1-methyl butyl, isohesyl, 2-ethylhexyl, 2-methyl hexyl, cyclohexyl, cyclopentyl, 2-norborny.The linear alkyl that wherein more preferably contains 1～12 carbon atom contains the branched-alkyl of 3～12 carbon atoms, contains the naphthenic base of 5～10 carbon atoms.
For the substituting group that this alkyl can contain, can use the group of the monovalence nonmetallic atom group that contains except that hydrogen atom.Its preferred embodiment be halogen atom (as-F ,-Br ,-Cl; with-I), hydroxyl, alkoxy; aryloxy group, sulfydryl, alkylthio group; arylthio, alkyl disulfide group, aryl disulfide group; amino, N-alkyl amino, N; the N-dialkyl amido, N-arylamino, N; the N-ammonia diaryl base, N-alkyl-N-arylamino, acyloxy; carbamoyloxy, N-alkyl carbamoyloxy base, N-arylamino formyloxy; N, N-dialkyl amido formyloxy, N; N-ammonia diaryl base formyloxy, N-alkyl-N-arylamino formyloxy, alkyl sulfide oxygen base (sulfoxy); aryl sulphur oxygen base, acyl sulfenyl, acylamino-; the N-alkyl amido; N-aryl acylamino-, urea groups, N '-alkyl urea groups; N '; N '-dialkyl group urea groups, N '-aryl-ureido, N '; N '-diaryl urea groups; N '-alkyl-N '-aryl-ureido, N-alkyl urea groups, N-aryl-ureido; N '-alkyl-N-alkyl urea groups; N '-alkyl-N-aryl-ureido, N ', N '-dialkyl group-N-alkyl urea groups; N '; N '-dialkyl group-N-aryl-ureido, N '-aryl-N-alkyl urea groups, N '-aryl-N-aryl-ureido; N '; N '-diaryl-N-alkyl urea groups, N ', N '-diaryl-N-aryl-ureido; N '-alkyl-N '-aryl-N-alkyl urea groups; N '-alkyl-N '-aryl-N-aryl-ureido, alkoxycarbonyl amido, aryloxy carbonyl amino; N-alkyl-N-alkoxycarbonyl amido; N-alkyl-N-aryloxy carbonyl amino, N-aryl-N-alkoxycarbonyl amido, N-aryl-N-aryloxy carbonyl amino; formoxyl; acyl group, carboxyl, alkoxy carbonyl group; aryloxy carbonyl; carbamyl, N-alkyl-carbamoyl, N; N-dialkyl amido formoxyl; the N-aryl-amino-carbonyl, N, N-ammonia diaryl base formoxyl; N-alkyl-N-aryl-amino-carbonyl; alkyl sulphinyl, aryl sulfonyl kia, alkyl sulphonyl; aryl sulfonyl, sulfo group (SO 3H) and conjugation base (being called " sulfonic acid foundation " later on), alcoxyl sulfonyl, fragrant oxygen sulfonyl, ammonia sulfinyl (sulfinamoyl); N-alkyl ammonia sulfinyl, N, N-dialkyl amino sulfinyl, N-aryl ammonia sulfinyl; N, N-ammonia diaryl sulfinyl, N-alkyl-N-aryl ammonia sulfinyl; sulfamoyl, N-alkylsulfamoyl group, N; the N-dialkyl sulfamine, N-ammonia aryl sulfonyl, N; N-ammonia diaryl sulfonyl, N-alkyl-N-ammonia aryl sulfonyl, phosphono (PO 3H 2) and conjugation base (being called " phosphonic acids foundation " later on), dialkyl phosphine acyl group (PO 3(alkyl) 2), diaryl phosphono (PO 3(aryl) 2), alkylaryl phosphono (PO 3(alkyl) (aryl)), monoalkyl phosphono (PO 3H (alkyl)) and conjugation base (being called " alkyl phosphonic acid foundation " later on), single aryl phosphine acyl group (PO 3H (aryl)) and conjugation base (being called " arylphosphonic acid foundation " later on), phosphonato (OPO 3H 2) and conjugation base (being called " phosphonate radical closes the oxygen base " later on), dialkyl phosphine acyloxy (OPO 3(alkyl) 2), diaryl phosphonato (OPO 3(aryl) 2), alkylaryl phosphonato (OPO 3(alkyl) (aryl)), monoalkyl phosphonato (OPO 3H (alkyl)) and conjugation base (being called " the alkylphosphines acid group closes the oxygen base " later on), single aryl phosphine acyloxy (OPO 3H (aryl)) and conjugation base (being called " the aryl phosphine acid group closes the oxygen base " later on), cyano group, nitro, aryl, thiazolinyl, alkynyl, heterocyclic radical, silicyl.
As for the instantiation of alkyl in this substituting group, specifiable is above-mentioned alkyl. the instantiation of aryl comprises in the above-mentioned substituting group: phenyl, xenyl, naphthyl, tolyl, xylyl, 2,4, the 6-trimethylphenyl, cumenyl, chlorphenyl, bromophenyl, chloromethyl phenyl, hydroxyphenyl, anisyl, ethoxyphenyl, phenoxy phenyl, acetate phenyl, the benzoxy phenyl, methyl thio-phenyl, phenyl thio-phenyl, the methylamino phenyl, dimethylamino phenyl, acetylamino phenyl, carboxyl phenyl, methoxycarbonyl group phenyl, ethoxyphenyl carbonyl, the carbobenzoxy phenyl, N-phenyl amino formylphenyl, cyano-phenyl, the sulfo group phenyl, sulfonate radical closes phenyl, the phosphono phenyl, and phosphonate radical closes phenyl.
Also have, the example of thiazolinyl comprises: vinyl, 1-propenyl, 1-butenyl group, cinnamyl and 2-chloro-1-vinyl; The example of alkynyl comprises: ethinyl, 1-propinyl, 1-butynyl and trimethylsilyl ethinyl.As for acyl group (R 01CO-) R in 01, what can enumerate is hydrogen atom and abovementioned alkyl and aryl.In these substituting groups, more preferably halogen atom (for example-F ,-Br ,-Cl and-I); alkoxy, aryloxy group, alkylthio group, arylthio; the N-alkyl amino, N, N-dialkyl amido, acyloxy; N-alkyl carbamoyloxy base, N-arylamino formyloxy, acylamino-, formoxyl; acyl group, carboxyl, alkoxy carbonyl group; aryloxy carbonyl, carbamyl, N-alkyl-carbamoyl; N, N-dialkyl amido formoxyl, N-aryl-amino-carbonyl; N-alkyl-N-aryl-amino-carbonyl, sulfo group, sulfonic acid foundation; sulfamoyl, N-alkylsulfamoyl group, N; the N-dialkyl sulfamine, N-ammonia aryl sulfonyl, N-alkyl-N-ammonia aryl sulfonyl; phosphono, phosphonic acids foundation, dialkyl phosphine acyl group; the diaryl phosphono, an alkylphosphines acyl group, alkyl phosphonic acid foundation; one aryl phosphine acyl group, arylphosphonic acid foundation, phosphonato; phosphonate radical closes the oxygen base, aryl, and thiazolinyl.The heterocyclic radical of enumerating has pyridine radicals and piperidyl; As for silicyl, can enumerate trimethylsilyl.On the other hand, as for the alkylidene in the substituted alkyl, can enumerate is that the above-mentioned alkyl that contains 1～20 carbon atom is removed behind any one hydrogen atom and the organic residue of divalence that obtains.Wherein preferably contain the linear alkylene of 1～12 carbon atom, contain the sub-branched alkyl of 3～12 carbon atoms, and the cyclic alkylidene that contains 5～10 carbon atoms.The preferred embodiment of the substituted alkyl that the combination of this substituting group and alkylidene is obtained comprises: chloromethyl, bromomethyl, the 2-chloroethyl, trifluoromethyl, methoxyl methyl, the different third oxygen methyl, fourth oxygen methyl, the second month in a season-the Ding oxygen-butyl, methoxy (ethoxy) ethyl, allyloxy methyl, Phenoxymethyl, methylthiomethyl, tolyl sulphomethyl, pyridylmethyl, the tetramethyl piperidine ylmethyl, N-acetyl tetramethyl piperidine ylmethyl, trimethylsilyl methyl, methoxyethyl, the ethylamino ethyl, the diethylamino propyl group, morpholino propyl group, acetyl-o-methyl, the benzoxy methyl, N-cyclohexyl carboxyamide oxygen base ethyl, N-phenyl amino formyloxy ethyl, acetylamino ethyl, N-toluyl aminopropyl, the 2-oxoethyl, 2-oxopropyl, carboxyl propyl group, the methoxycarbonyl group ethyl, the allyloxycarbonyl butyl, chlorobenzene oxygen carbonyl methyl, carbamoyl methyl, N-methylamino formyl ethyl, N, N-dipropyl carbamoyl methyl, N-(anisyl) carbamyl ethyl, N-methyl-N-(sulfophenyl) carbamoyl methyl, the sulphur butyl, sulfonate radical closes butyl, the sulfonamide butyl, N-ethyl sulfonamide methyl, N, N-dipropyl sulfonamide propyl group, N-amino toluene sulphonyl propyl group, N-methyl-N-(phosphono phenyl) sulfonamide octyl group, the phosphono butyl, phosphonate radical closes hexyl, diethyl phosphono butyl, diphenyl phosphono propyl group, methyl phosphono butyl, the methylphosphine acid group closes butyl, toluene phosphono hexyl, the toluene phosphonate radical closes hexyl, phosphono oxygen propyl group, phosphonate radical closes oxygen-butyl, benzyl, phenethyl, α-Jia Jibianji, 1-methyl isophthalic acid-phenethyl, right-methyl-benzyl, cinnamyl, allyl, 1-propenyl methyl, 2-butenyl group, the 2-methacrylic, 2-metering system ylmethyl, 2-propynyl, 2-butynyl and 3-butynyl.
As for aryl, specifiable is phenyl ring, 2 or 3 condensed ring that phenyl ring forms, and the condensed ring of the unsaturated ring formation of phenyl ring and 5-unit.Instantiation comprises: phenyl, naphthyl, anthryl, phenanthryl, indenyl, acenaphthenyl, fluorenyl.Wherein, preferred phenyl and naphthyl.
As for substituted aryl, use be on one or more one-tenth ring carbon atoms of above-mentioned aryl, to have to contain except that hydrogen atom other monovalence nonmetallic atom group as substituent aryl.Substituent preferred embodiment comprises above-mentioned alkyl and substituted alkyl, and as the substituting group in the above-mentioned substituted alkyl and by the group enumerated.
The preferred embodiment of substituted aryl comprises: xenyl, tolyl, xylyl, 2,4, the 6-trimethylphenyl, cumenyl, chlorphenyl, bromophenyl, fluorophenyl, chloromethyl phenyl, trifluoromethyl, hydroxyphenyl, anisyl, methoxy (ethoxy) phenyl, the allyloxy phenyl, phenoxy phenyl, methyl thio-phenyl, the toluene thio-phenyl, ethylamino phenyl, lignocaine phenyl, the morpholino phenyl, acetyl oxygen phenyl, benzoyl oxygen phenyl, N-cyclohexyl carboxyamide oxygen phenyl, N-phenyl amino methanoyl phenyl, acetylamino phenyl, N-toluyl aminophenyl, carboxyl phenyl, methoxycarbonyl group phenyl, allyloxycarbonyl phenyl, chlorobenzene oxygen carbonyl phenyl, the carbamyl phenyl, N-methylamino formylphenyl, N, N-dipropyl carbamyl phenyl, N-(anisyl) carbamyl phenyl, N-methyl-N-(sulfophenyl) carbamyl phenyl, sulfo group phenyl, sulfonate radical closes phenyl, sulfamoyl phenyl, N-ethyl sulfamoyl phenyl, N, N-dipropyl sulfamoyl phenyl, N-tolyl sulfamoyl phenyl, N-methyl-N-(phosphono phenyl) sulfamoyl phenyl, phosphono phenyl, phosphonate radical closes phenyl, diethyl phosphono phenyl, diphenyl phosphono phenyl, methyl phosphono phenyl, the methylphosphine acid group closes phenyl, tolyl phosphono phenyl, the tolylphosphine acid group closes phenyl, allyl phenyl, 1-propenyl aminomethyl phenyl, 2-butenyl group phenyl, 2-methacrylic phenyl, 2-methylpropenyl phenyl, 2-propyl group phenyl, 2-butynyl phenyl and 3-butynyl phenyl.
As for thiazolinyl, substituted alkenyl, alkynyl and substituted alkynyl (C (R 02)=C (R 03) (R 04) and-C C (R 05)), operable is R in the group 02, R 03, R 04And R 05Each all represents the group that contains the monovalence nonmetallic atom group.R 02, R 03, R 04And R 05Preferred embodiment comprise: hydrogen atom, halogen atom, alkyl, substituted alkyl, aryl and substituted aryl.Its instantiation comprises those groups of before having enumerated.R 02, R 03, R 04And R 05More preferably example comprise: hydrogen atom, halogen atom contains linearity, branching or the cyclic alkyl of 1～10 carbon atom.
The instantiation of thiazolinyl, substituted alkenyl, alkynyl and substituted alkynyl comprises: vinyl, 1-propenyl, 1-butenyl group, the 1-pentenyl, 1-hexenyl, 1-octenyl, 1-methyl isophthalic acid-propenyl, 2-methyl isophthalic acid-propenyl, 2-methyl-1-butene thiazolinyl, 2-phenyl-1-vinyl, 2-chloro-1-vinyl, ethinyl, 1-propinyl, 1-butynyl and phenylacetylene base.As for heterocyclic radical, specifiable is as the substituent pyridine radicals of substituted alkyl.
As for above-mentioned substituted oxy (R 06O-) in, can use R 06The group that contains the monovalence nonmetallic atom group except that hydrogen atom of representative.The preferred embodiment of substituted oxy comprises: alkoxy, aryloxy group, acyloxy, carbamoyloxy, N-alkyl carbamoyloxy base, N-arylamino formyloxy, N, N-dialkyl amido formyloxy, N, N-ammonia diaryl base formyloxy, N-alkyl-N-arylamino formyloxy, alkyl sulfide oxygen base, aryl sulphur oxygen base, phosphonato and phosphonate radical close the oxygen base.As for alkyl in these groups and aryl, specifiable is above-mentioned alkyl, substituted alkyl, aryl and substituted aryl.Also have, as for the acyl group (R in the acyloxy 07CO-), specifiable is R wherein 07Represent the acyl group of abovementioned alkyl, substituted alkyl, aryl or substituted aryl.In these substituting groups, more preferably alkoxy, aryloxy group, acyloxy and aryl sulphur oxygen base.The instantiation of preferred substituted oxy comprises: methoxyl, ethoxy, propoxyl group, isopropoxy, butoxy, amoxy, own oxygen base, dodecyloxy, benzyloxy, allyloxy, benzene ethoxy, the carboxyl ethoxy, methoxycarbonyl group ethoxy, carbethoxyl group ethoxy, methoxyethoxy, benzene oxygen ethoxy, methoxy (ethoxy) ethoxy, ethoxy ethoxy ethoxy, morpholino ethoxy, morpholino propoxyl group, allyl oxygen ethoxy ethoxy, phenoxy group, toloxyl, xylyloxy, 2,4,6-front three phenoxy group, cumenyl oxygen base, methoxy phenoxy, the ethoxy phenoxy group, chlorophenoxy, bromine phenoxy group, acetoxyl group, benzoyloxy, naphthoxy, the phenyl sulfonyloxy, phosphonato, phosphonate radical close the oxygen base.Substituted-amino (R as for amide-containing 08NH-or (R 09) (R 010) N-), can use R 08, R 09And R 010Representative contains the group of the monovalence nonmetallic atom group except that hydrogen atom separately.Additional disclosure once, R 09And R 010Can be incorporated into ring. the preferred embodiment of substituted-amino comprises: the N-alkyl amino; N; the N-dialkyl amido; the N-arylamino; N, N-ammonia diaryl base, N-alkyl-N-arylamino; acylamino-; the N-alkyl amido, N-aryl acylamino-, urea groups; N '-alkyl urea groups; N ', N '-dialkyl group urea groups, N '-aryl-ureido; N '; N '-diaryl urea groups, N '-alkyl-N '-aryl-ureido, N-alkyl urea groups; the N-aryl-ureido; N '-alkyl-N-alkyl urea groups, N '-alkyl-N-aryl-ureido, N '; N '-dialkyl group-N-alkyl urea groups; N '-alkyl-N '-aryl-ureido, N ', N '-dialkyl group-N-alkyl urea groups; N '; N '-dialkyl group-N '-aryl-ureido, N '-aryl-N-alkyl urea groups, N '-aryl-N-aryl-ureido; N '; N '-diaryl-N-alkyl urea groups, N ', N '-diaryl-N-aryl-ureido; N '-alkyl-N '-aryl-N-alkyl urea groups; N '-alkyl-N '-aryl-N-aryl-ureido, alkoxycarbonyl amido, aryloxy carbonyl amino; N-alkyl-N-alkoxycarbonyl amido; N-alkyl-N-aryloxy carbonyl amino, N-aryl-N-alkoxycarbonyl amido, and N-aryl-N-aryloxy carbonyl amino. as for alkyl in these groups and aryl; specifiable is above-mentioned alkyl; substituted alkyl; aryl and substituted aryl. same, acylamino-; acyl group (R in N-alkyl amido and the N-aryl acylamino- 07CO-) R 07As discussed previously.Wherein, more preferably N-alkyl amino, N, N-dialkyl amido, N-arylamino and acylamino-.The instantiation of preferred substituted-amino comprises: methylamino, ethylamino, lignocaine, morpholino base, piperidino, pyrrolidinyl (pyrrolidino), phenylamino, benzamido, and acetylamino.As for substituted sulphonyl (R 011-SO 2-), can use wherein R 011Representative contains the substituted sulphonyl of the group of monovalence nonmetallic atom group.Its preferred example comprises alkyl sulphonyl and aryl sulfonyl.As for alkyl in these groups and aryl, what can enumerate is cited those in above-mentioned alkyl, substituted alkyl, aryl and the substituted aryl.The instantiation of this substituted sulphonyl comprises: fourth sulfonyl, benzenesulfonyl, chlorobenzene sulfonyl.
Sulfonic acid foundation (SO 3 -) refer to previous described sulfo group (SO 3H) conjugate base negative ion, general preferred anionic group and balance cation use together.This balance cation that can enumerate generally is known kation, that is: various salt (for example ammonium, Liu ， Phosphonium, iodine and azine), and metallic ion (for example, Na +, K +, Ca 2+And Zn 2+).
As for substituted carbonyl (R 013-CO-), can use wherein R 013Representative contains those of group of monovalence nonmetallic atom group.The preferred embodiment of substituted carbonyl comprises: formoxyl, acyl group, carboxyl, alkoxy carbonyl group, aryloxy carbonyl; carbamyl, N-alkyl-carbamoyl, N, N-dialkyl amido formoxyl; the N-aryl-amino-carbonyl, N, N-ammonia diaryl base formoxyl, and N-alkyl-N '-aryl-amino-carbonyl.As for alkyl in these groups and aryl, those that above-mentioned alkyl, substituted alkyl, aryl and the substituted aryl of the conduct that can enumerate is cited.In these substituted carbonyls, more preferably formoxyl, acyl group, carboxyl, alkoxy carbonyl group, aryloxy carbonyl, carbamyl, N-alkyl-carbamoyl, N, N-dialkyl amido formoxyl and N-aryl-amino-carbonyl; Also more preferably formoxyl, acyl group, alkoxy carbonyl group and aryloxy carbonyl.The instantiation of preferred substituted carbonyl comprises: formoxyl, acetyl group, benzoyl; carboxyl, methoxycarbonyl group, carbethoxyl group; allyloxycarbonyl; dimethylamino phenethyl carbonyl, methoxycarbonyl group methoxycarbonyl group, N-methylamino formoxyl; N-phenyl amino formoxyl; N, N-diethylamino formoxyl, and morpholino carbonyl.
As for substituted sulfinyl (R 014-SO-), can use wherein R 014Representative contains the substituted sulfinyl of the group of monovalence nonmetallic atom group.Its preferred embodiment comprises: alkyl sulphinyl, aryl sulfonyl kia, ammonia sulfinyl, N-alkyl ammonia sulfinyl, N, N-dialkyl amino sulfinyl, N-aryl ammonia sulfinyl, N, N-ammonia diaryl sulfinyl, and N-alkyl-N-aryl-ammonia sulfinyl.As for alkyl in these groups and aryl, what can enumerate is as cited those of above-mentioned alkyl, substituted alkyl, aryl and substituted aryl.Wherein preferred alkyl sulfinyl and aryl sulfonyl kia.The instantiation of substituted sulfinyl comprises: hexyl sulfinyl, benzyl sulfinyl and tolyl sulfinyl.
Alleged herein replacement phosphono is meant the phosphono that one or two hydroxyl on the phosphono is replaced by other organic oxo base.Its preferred embodiment comprises: above-mentioned dialkyl phosphine acyl group, diaryl phosphono, alkylaryl phosphono, an alkylphosphines acyl group and an aryl phosphine acyl group.Wherein more preferably dialkyl phosphine acyl group and diaryl phosphono.Instantiation comprises diethyl phosphonyl, dibutyl phosphono and diphenylphosphine acyl group.Phosphonic acids foundation (the PO that herein mentions 3H 2-or PO 3H-) referring to the conjugate base anion base of phosphono, is from phosphono (PO 3H 2) the first time acid dissociation or for the second time acid dissociation derive and obtain.Usually preferably anion base and balance cation are used together.This balance cation that can enumerate is usually known kation, that is: various salt (for example ammonium, Liu ， Phosphonium, iodine and azine), and metallic ion (for example, Na +, K +, Ca 2+And Zn 2+).
The replacement phosphonic acids foundation of herein mentioning refers to the conjugate base anion base that a hydroxyl on the above-mentioned phosphono is replaced by organic oxo base.Instantiation comprises an above-mentioned alkylphosphines acyl group (PO 3H (alkyl)) and an aryl phosphine acyl group (PO 3H (aryl)) conjugate base.
Then, X in the above-mentioned formula (I) and the X in the above-mentioned formula (I-2) below will be described 1X represents to be selected from :-O-,-S-,-SO 2-,-NH-,-N (R 3)-and-divalent linker of CO-.In the middle of these, consider from the sensitivity viewpoint, preferred-O-,-S-,-NH-,-N (R 3)-, and preferred especially-O-and-N (R 3)-.X 1Expression is selected from :-O-,-S-,-SO 2-,-NH-,-N (R 3)-,-CH 2-,-CH (R 4)-and-C (R 4) (R 5)-divalent linker.In the middle of these, consider from the sensitivity viewpoint, preferred-NH-,-N (R 3)-,-CH 2-,-CH (R 4)-and-C (R 4) (R 5)-; And more preferably-NH-and-N (R 3)-.Consider from sensitivity and storage stability, most preferably-N (R 3)-.
Here, the R among the foregoing X 3With foregoing X 1In R 3, R 4And R 5Represent hydrogen atom or monovalence substituting group independently of one another.R in monovalence substituting group and the foregoing formula (I) 1And R 2In monovalence substituting group implication identical.
Particularly, preferred R 3The expression alkyl, alkenyl, alkynyl group, aryl, perhaps heterocyclic radical, each in these groups can have substituting group.In addition, preferred R 3In its structure, contain-CO 2-and-CON (R 8)-at least one.R 3Most preferred structure is such structure, and it has by the ester structure of following formula (i) expression and the amide structure of (ii) being represented by following formula.Especially, preferably have those of the amide structure (ii) represented by following formula:
In the foregoing formula, R 6, R 7And R 8Represent hydrogen atom or monovalence substituting group independently of one another; And Z represents the monovalence substituting group.Monovalence substituting group and foregoing formula (I) and (I-2) in R 1And R 2Monovalence substituting group implication identical.
In addition, foregoing X 1In, by R 4And R 5The monovalence substituting group of expression and foregoing formula (I) and (I-2) middle R 1And R 2Monovalence substituting group implication identical.
The instantiation (A-1) that below will provide the monocarboxylic acid compound of being represented by formula (I-2) still is to be understood that the present invention is not limited to these to (A-87).
Figure G2004100070091D00241
Figure G2004100070091D00261
Figure G2004100070091D00281
Figure G2004100070091D00291
In addition, other preferred embodiment as compound (A), what can enumerate is: have a kind of like this compound by following formula (I-3) expression of structure, the structure that the ring structure that the A in the compound of promptly foregoing formula (I-2) expression represents is connected with a plurality of groups of being represented by formula (I):
Wherein
A, R 1And R 2Identical with those implications of formula (I).But, R 1And R 2At least one is a carboxyl, contains the alkyl of 1 to 10 carbon atom or contains the alkyl of holding carboxyl and containing 1 to 10 carbon atom.N represents 2 to 6 integer.
Then, below will illustrate the synthetic embodiment of representativeness, but be to be understood that the present invention is not limited to these according to the monocarboxylic acid compound by formula (I-2) expression of the present invention.
To illustrate the synthetic embodiment of representativeness of monocarboxylic acid compound of the present invention below, but be to be understood that the present invention is not limited to this.
Synthesizing of＜compound (A-24) 〉
The N-phenylimino oxalic acid that adds 62.8g in 2 liters of eggplant type flasks flows down at nitrogen it is dissolved in the 500mL toluene, then to the acetic anhydride that wherein adds 32.0g.The reflux potpourri also stirs.After one hour, reaction mixture is cooled to room temperature, in potpourri, adds the 3L hexane while stirring and precipitate.The filtering reaction product obtains the N-phenylimino diethyl acid anhydrides of 52.0g.Then, the N-phenylimino diethyl acid anhydrides of 5.1g gained is flowed down in the eggplant type flask of the 200mL that packs at nitrogen, in bottle, add 60mL methyl alcohol then.After at room temperature stirring 6 hours, distillation removes and desolvates under vacuum.(eluting solvent: hexane/ethyl acetate) purifying obtains the compound (A-24) of 5.7g to residue through silica gel column chromatography.The compound of gained turns out to be compound (A-24) through NMR, IR and mass spectrophotometry.
Synthesizing of＜compound (A-52) 〉
The N-phenylimino oxalic acid that adds 62.8g in 2 liters of eggplant type flasks flows down at nitrogen it is dissolved in the 500mL toluene, then to the acetic anhydride that wherein adds 32.0g.The reflux potpourri also stirs.After one hour, reaction mixture is cooled to room temperature, in potpourri, adds the 3L hexane while stirring and precipitate.The filtering reaction product obtains the N-phenylimino diethyl acid anhydrides of 52.0g.
Then, the N-phenylimino diethyl acid anhydrides of 5.1g gained is flowed down in the eggplant type flask of the 200mL that packs at nitrogen, then to wherein adding 50mL benzylalcohol.After at room temperature stirring 8 hours, distillation removes and desolvates under vacuum.(eluting solvent: hexane/ethyl acetate) purifying obtains the compound (A-52) of 7.2g to residue through silica gel column chromatography.The compound of gained turns out to be compound (A-52) through NMR, IR and mass spectrophotometry.
Synthesizing of＜compound (A-55) 〉
The N-phenylimino oxalic acid that adds 62.8g in 2 liters of eggplant type flasks flows down at nitrogen it is dissolved in the 500mL toluene, then to the acetic anhydride that wherein adds 32.0g.The reflux potpourri also stirs.After one hour, reaction mixture is cooled to room temperature, in potpourri, adds the 3L hexane while stirring and precipitate.The filtering reaction product obtains the N-phenylimino diethyl acid anhydrides of 52.0g.
Then, the N-phenylimino diethyl acid anhydrides of 5.1g gained is flowed down in the eggplant type flask of the 200mL that packs at nitrogen, in bottle, add 1-methoxyl-2-propyl alcohol of 50mL then.After at room temperature stirring 4 hours, distillation removes and desolvates under vacuum.(eluting solvent: hexane/ethyl acetate) purifying obtains the compound (A-55) of 6.0g to residue through silica gel column chromatography.The compound of gained turns out to be compound (A-55) through NMR, IR and mass spectrophotometry.
Can use separately according to previous described The compounds of this invention (A) or (A-1) or its two or more mix to use. from the susceptibility of abundant raising with guarantee that the splendid elimination aspect in territory, non-exposed area considers, based on the polymerisable compound total solid weight, the addition of compound (A) etc. can be 0.1 to 70 weight %, be preferably 0.5 to 50 weight %, and more preferably 1 to 30 weight %. former described addition is used as to the polymerisable compound that has wherein added compound (A) etc. under the situation of recording materials of Lighographic printing plate precursor, can obtain following benefit: can carry out record in high sensitive ground, stain in the non-image areas generation when preventing to print, and improved before the recording layer curing significantly and film physical property afterwards.
[(B) radical initiator]
Polymerisable compound of the present invention is characterised in that and contains radical initiator.The radical initiator of herein mentioning is meant the compound that produces the polyreaction of the described after a while compound (C) (polymerizable compound) that contains an alkene formula unsaturated link at least of free radical, initiation and acceleration by the energy of light and/or heating.
Among the present invention, the preferred embodiment of radical initiator comprises: (a) aromatic ketone, (b) salt compound, (c) organic peroxide, (d) thio-compounds, (e) Hexaarylbiimidazole compound, (f) ketoxime ester compounds, (g) borate compound, (h) azines, (i) Metallocenic compound, (j) active ester compound, (k) contain the compound of carbon-halogen bond, and (l) azo-based compound.Although will provide the instantiation of above-mentioned (a)～(l) below, be to be understood that the present invention is not limited to these compounds.
(a) aromatic ketone:
As for preferred aromatic ketone (a) as the used radical initiator of the present invention, specifiable is to have RADIATION CURING IN POLYMER SCIENCE AND TECHNOLOGY, J.P.Fousassier and J.F.Rabek (1993), the compound of the described hexichol of 77-117 page or leaf (first) ketone skeleton or thioxanthones skeleton.The following compound of for example enumerating.
At first, as the example of particularly preferred aromatic ketone (a), can enumerate the benzoin ether compound described in the α described in the JP-B-47-6416-thiobenzophenone compound and the JP-B-47-3981, for example following compound:
Figure G2004100070091D00351
The benzoin compound of the alpha-substituted described in the JP-B-47-22326, specifiable have a for example following compound:
Benzoin derivatives described in the JP-B-47-23664, the aroyl phosphonate ester described in the JP-A-57-30704, and the dialkoxy benzophenone described in the JP-B-60-26483, for example following compound:
Benzoin ether described in JP-B-60-26403 and the JP-B-62-81345, can enumerate for example following compound:
Alpha-amido benzophenone described in JP-B-1-34242, USP 4,318,791 and the European patent 0284561A1, can enumerate for example following compound:
Right-two (dimethylamino benzoyl) benzene described in the JP-A-2-211452, can enumerate for example following compound:
The aromatic ketone that sulphur described in the JP-A-61-194062 replaces, can enumerate for example following compound:
Figure G2004100070091D00372
Acylphosphanes sulfide described in the JP-B-2-9597, can enumerate for example following compound:
Acylphosphanes described in the JP-B-2-9596, can enumerate for example following compound:
Figure G2004100070091D00374
Also can enumerate the cumarin described in thioxanthones described in the JP-B-63-61950 and the JP-B-59-42864.
(b) salt compound:
As the salt compound (b) of the used radical initiator of the present invention, can be listed below the compound of molecular formula (1)～(3) representative as for preferably.
Molecular formula (1)
Ar 1-I +-Ar 2 (Z 2) -
Molecular formula (2)
Ar 3-N +≡N (Z 3) -
Molecular formula (3)
In the molecular formula (1), Ar 1And Ar 2Representative independently of one another contains the aryl of the optional replacement that is no more than 20 carbon atoms.When this aryl had substituting group, substituent preferred embodiment comprised: halogen atom, nitro contains the alkyl that is no more than 12 carbon atoms, contains the alkoxy that is no more than 12 carbon atoms, and contains the aryloxy group that is no more than 12 carbon atoms.(Z 2) -Representative is selected from the counterion of following group: halide ion, high chloro acid ion, carboxylic acid ion, tetrafluoro boric acid salt ion, hexafluorophosphoric acid salt ion, and azochlorosulfonate acid ion, preferred high chloro acid ion, hexafluorophosphoric acid salt ion and aryl sulfonic acid ion.
In the molecular formula (2), Ar 3Representative contains the aryl of the optional replacement that is no more than 20 carbon atoms.Substituent preferred embodiment comprises: halogen atom, nitro, contain the alkyl that is no more than 12 carbon atoms, contain the alkoxy that is no more than 12 carbon atoms, contain the aryloxy group that is no more than 12 carbon atoms, contain the alkylamino that is no more than 12 carbon atoms, contain the dialkyl amido that is no more than 12 carbon atoms, it is amino to contain the virtue that is no more than 12 carbon atoms, and contains the ammonia diaryl base that is no more than 12 carbon atoms.(Z 3) -Representative and (Z 2) -The counterion that implication is identical.
In the molecular formula (3), R 23, R 24And R 25Can be identical or differ from one another, representative contains the alkyl of the optional replacement that is no more than 20 carbon atoms separately.Substituent preferred embodiment comprises: halogen atom, nitro contains the alkyl that is no more than 12 carbon atoms, contains the alkoxy that is no more than 12 carbon atoms, and contains the aryloxy group that is no more than 12 carbon atoms.(Z 4) -Representative and (Z 2) -The counterion that implication is identical.
The instantiation that goes for salt of the present invention comprises the salt described in the following file: [0030]～[0033] section among the Japanese patent application 11-310623, [0015]～[0046] section among the Japanese patent application 2000-160323, and the special fragrant sulfonium salt compound described in Japanese patent application 2000-266797,2001-177150,2000-160323,2000-184603,2000-310808,2002-265467 and the 2002-366539, all these patented claims all propose by this assignee is previous.
The maximum absorption wavelength that is preferred for salt of the present invention is no more than 400nm, more preferably no more than 360nm.
When absorbing wavelength is positioned at the ultraviolet region, can under white light, handle Lighographic printing plate precursor.
(c) organic peroxide:
As for preferred organic peroxide (c) as radical initiator of the present invention; comprising nearly all organic compound that in molecule, contains an o-o bond at least. the example comprises: methyl ethyl ketone peroxide; cyclohexanone peroxide; 3; 3; 5-trimethyl-cyclohexanone superoxide; the peroxidating methyl cyclohexanone, acetylacetone peroxide, 1; two (t-butyl peroxy)-3 of 1-; 3,5-trimethylcyclohexanone, 1; two (t-butyl peroxy) cyclohexanone of 1-; 2, two (t-butyl peroxy) butane of 2-, tert-butyl hydroperoxide; cumene hydroperoxide; two-cumene hydroperoxide hydrogen, right-the methane hydrogen peroxide, 2; 5-dimethylhexane-2; 5-diperoxy hydrogen, 1,1; 3; the 3-tetramethyl butyl hydroperoxide, di-tert-butyl hydrogen peroxide, tert-butyl group cumyl peroxide; dicumyl peroxide; two (t-butyl peroxy isopropyl) benzene, 2,5-dimethyl-2; 5-two (t-butyl peroxy) hexane; 2,5-xanoyl superoxide, amber () acidylate peroxide; benzoyl peroxide; 2,4-dichloro-benzoyl superoxide ,-the toluoyl superoxide; diisopropyl peroxydicarbonate; two-2-ethylhexyl peroxide, two carbonic esters, two-2-ethoxyethyl peroxide, two carbonic esters, dimethoxy isopropyl peroxy carbonates; two (3-methyl-3-methoxy-butyl) peroxide two carbonic esters; tert-butyl peroxy acetate, t-butylperoxy pivarate, the peroxide neodecanoic acid tert-butyl ester; the Peroxycaprylic acid tert-butyl ester; t-butyl peroxy-3,5,5-tri-methyl hexanoic acid ester; the peroxide lauric acid tert-butyl ester; the tertiary carbon hydrochlorate, 3,3 '; 4; 4 '-four (t-butyl peroxy carbonyl) benzophenone, 3,3 '; 4; 4 '-four (tertiary pentyl peroxide carbonyl) benzophenone, 3,3 '; 4; 4 '-four (uncle's hexyl peroxide carbonyl) benzophenone, 3,3 '; 4; 4 '-four (uncle's octyl group peroxide carbonyl) benzophenone, 3,3 '; 4; 4 '-four (cumyl peroxide carbonyl) benzophenone, 3,3 '; 4; 4 '-four (right-isopropyl cumyl peroxide carbonyl) benzophenone, carbonyl two (t-butyl peroxy dihydrophthalic acid ester), and carbonyl two (uncle's hexyl peroxide dihydrophthalic acid ester).
Wherein, preferred ester superoxide, for example 3,3 ', 4,4 '-four (t-butyl peroxy carbonyl) benzophenone, 3,3 ', 4,4 '-four (tertiary pentyl peroxide carbonyl) benzophenone, 3,3 ', 4,4 '-four (uncle's hexyl peroxide carbonyl) benzophenone, 3,3 ', 4,4 '-four (uncle's octyl group peroxide carbonyl) benzophenone, 3,3 ', 4,4 '-four (cumyl peroxide carbonyl) benzophenone, 3,3 ', 4,4 '-four (right-isopropyl cumyl peroxide carbonyl) benzophenone, and di-t-butyl diperoxy isophthalic acid ester.
(d) thio-compounds:
As for the thio-compounds that is preferably used as radical initiator of the present invention (d), specifiable is the compound with following molecular formula (4) representative structure.
Molecular formula (4)
Herein, R 26Represent alkyl, aryl or substituted aryl; R 27Represent hydrogen atom or alkyl.Equally, R 26And R 27Representative forms 5 yuan or 7 yuan of necessary nonmetallic atom groups of ring together, can choose wantonly in this ring to comprise the heteroatoms that is selected from oxygen atom, sulphur atom and nitrogen-atoms.
In the above-mentioned molecular formula (4), alkyl is preferably the alkyl that contains 1～4 carbon atom.Equally, preferred aryl groups is the aryl that contains 6～10 carbon atoms, for example phenyl and naphthyl.Substituted aryl comprises: above-mentioned aryl, but these aryl by halogen atom, for example the chlorine atom replaces; Alkyl, for example methyl; Perhaps alkoxy, for example methoxyl and ethoxy.R 27Be preferably the alkyl that contains 1～4 carbon atom.The instantiation of the thio-compounds of molecular formula (4) representative is listed below.
(e) Hexaarylbiimidazole compound:
The preferred Hexaarylbiimidazole compound (e) of the radical initiator that uses as the present invention, that enumerates has the lophine dimer described in JP-B-45-37377 and the JP-B-44-86516, for example 2,2 '-two (neighbour-chlorphenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, 2,2 '-two (neighbour-bromophenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, 2,2 '-two (neighbours, right-dichlorophenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, 2,2 '-two (neighbour-chlorphenyl)-4,4 ', 5,5 '-four (-anisyl) diimidazole, 2,2 '-two (neighbour, neighbour '-dichlorophenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, 2,2 '-two (o-nitrophenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, 2,2 '-two (neighbour-aminomethyl phenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole, and 2,2 '-two (neighbour-trifluorophenyl)-4,4 ', 5,5 '-tetraphenyl diimidazole.
(f) ketoxime ester compounds:
As for the ketoxime ester compounds (f) that is preferably used as radical initiator of the present invention, what enumerate is following compound:
3-benzoyl oxyimino group fourth-2-ketone, 3-acetyl oxyimino group fourth-2-ketone, 3-propionyl oxyimino group fourth-2-ketone, 2-acetyl oxyimino group penta-3-ketone, 2-acetyl oxyimino group-1-phenyl third-1-ketone, 2-benzoyl oxyimino group-1-phenyl third-1-ketone, 3-tolysulfonyl oxyimino group fourth-2-ketone, and 2-ethoxy carbonyl oxyimino group-1-phenyl third-1-ketone.
(g) borate compound:
As for the borate compound that is preferably used as radical initiator of the present invention (g), what enumerate is the compound of following molecular formula (5) representative.
Molecular formula (5)
Figure G2004100070091D00421
Here, R 28, R 29, R 30And R 31Can be identical or differ from one another, representative replaces or unsubstituted alkyl separately, replaces or unsubstituted aryl, replaces or unsubstituted thiazolinyl, replaces or unsubstituted alkynyl, perhaps replace or unsubstituted heterocyclic, and R 28, R 29, R 30And R 31In two or morely can be combined together to form ring texture.But, R 28, R 29, R 30And R 31In have at least a representative to replace or unsubstituted alkyl.(Z 5) +Represent alkali metal cation or quaternary ammonium cation.
R 28, R 29, R 30And R 31The examples of alkyl of representative comprises linearity, branching or naphthenic base, and preferably these alkyl contain 1～18 carbon atom.Instantiation comprises: methyl, ethyl, propyl group, isopropyl, butyl, amyl group, hexyl, octyl group, stearyl, cyclobutyl, cyclopentyl and cyclohexyl.The example of substituted alkyl also comprises abovementioned alkyl, but these alkyl are replaced by following group: halogen atom (for example-Cl and-Br), cyano group, nitro, aryl (being preferably phenyl), hydroxyl ,-COOR 32(R wherein 32Represent hydrogen atom, perhaps contain the alkyl or aryl of 1～14 carbon atom) ,-OCOR 33Or-OR 34(R wherein 33And R 34Representative contains the alkyl or aryl of 1～14 carbon atom separately), the substituting group of perhaps following molecular formula representative.
Figure G2004100070091D00431
Here, R 35And R 36Represent hydrogen atom independently of one another, perhaps contain the alkyl or aryl of 1～14 carbon atom.
R 28, R 29, R 30And R 31The aryl example of representative comprises the aryl that contains 1～3 ring, for example phenyl and naphthyl.The example of substituted aryl comprises above-mentioned aryl, but these aryl are replaced by above-mentioned substituted alkyl that contains 1～14 carbon atom or the substituting group in the aryl.R 28, R 29, R 30And R 31The example of the thiazolinyl of representative comprises linearity, branching or the cycloalkenyl group that contains 2～18 carbon atoms.The substituting group example of substituted alkenyl comprises the substituting group of enumerating in the above-mentioned substituted alkyl.R 28, R 29, R 30And R 31The example of the alkynyl of representative comprises linearity or the branching alkynyl that contains 2～28 carbon atoms.Substituent example comprises the substituting group of enumerating in the above-mentioned substituted alkyl in the substituted alkynyl.R 28, R 29, R 30And R 31The example of the heterocyclic radical of representative comprises the heterocycle more than 5 yuan or 5 yuan, is preferably 5～7 yuan of rings, and each heterocycle comprises among N, S and the O at least, and heterocycle can comprise condensed ring.In addition, heterocycle can contain the substituting group of enumerating in the above-mentioned substituted aryl.The instantiation of the compound of molecular formula (5) representative comprises USP 3,567,453 and 4,343,891 and European patent 109,772 and 109,773 described in compound, and following compound.
(h) azines:
As for the azines that is preferably used as radical initiator of the present invention (h), specifiable is JP-A-63-138345, JP-A-63-142345, JP-A-63-142346, the compound that contains a N-O key described in JP-A-63-143537 and the JP-B-46-42363.
(i) Metallocenic compound:
As for the Metallocenic compound that is preferably used as radical initiator of the present invention (i), specifiable is JP-A-59-152396, JP-A-61-151197, JP-A-63-41484, two cyclopentadiene titanium compounds described in JP-A-2-249 and the JP-A-2-4705, and the iron described in JP-A-1-304453 and the JP-A-1-152109-aromatic hydrocarbons complex.
The instantiation of above-mentioned two cyclopentadiene titanium compounds comprises: dicyclopentadienyl-Ti-dichloride, the two phenyl of dicyclopentadienyl-Ti-, dicyclopentadienyl-Ti-two-2,3,4,5,6-phenyl-pentafluoride-1-base, dicyclopentadienyl-Ti-two-2,3,5,6-phenyl tetrafluoride-1-base, dicyclopentadienyl-Ti-two-2,4,6-trifluoro-benzene-1-base, dicyclopentadienyl-Ti-2,6-two fluorobenzene-1-base, dicyclopentadienyl-Ti-two-2,4-two fluorobenzene-1-base, dimethyl cyclopentadienyl group-Ti-two-2,3,4,5,6-phenyl-pentafluoride-1-base, dimethyl cyclopentadienyl group-Ti-two-2,3,5,6-phenyl-pentafluoride-1-base, dimethyl cyclopentadienyl group-Ti-two-2,4-two fluorobenzene-1-base, two (cyclopentadienyl groups)-two (2,6 two fluoro-3-(pyridine-1-yl) phenyl) titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(methanesulfonamido) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(N-butyl two aromatic acylaminos) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(N-butyl-(4-chlorobenzoyl) amino) phenyl] titanium, two (cyclopentadienyl groups) two [2,6-two fluoro-3-(N-benzyl-2,2-dimethyl-penten acylamino-) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(N-(2-ethylhexyl)-4-tosyl) amino]-phenyl] titanium, two (cyclopentadienyl groups) two [2,6-two fluoro-3-(N-(3-Evil heptyl) benzamido) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(N-(3,6-two Evil decyls) benzamido) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(fluoroform sulfonamido) phenyl] titanium, two (cyclopentadienyl groups) two [2,6-two fluoro-3-(trifluoroacetamido) phenyl] titanium, two (cyclopentadienyl group) two [2,6-two fluoro-3-(2-chlorobenzoyl amino) phenyl] titanium, two (cyclopentadienyl groups) two [2,6-two fluoro-3-(4-chlorobenzoyl amino) phenyl] titanium, two (cyclopentadienyl group) two [2, (N-(3 for 6-two fluoro-3-, 6-Er Evil decyl)-2,2-dimethyl-penten acylamino-) phenyl] titanium, two (cyclopentadienyl group) two [2, (N-(3 for 6-two fluoro-3-, 7-dimethyl-7-methoxy octyl group) phenyl benzamido)] titanium, and two (cyclopentadienyl groups) two [2,6-two fluoro-3-(N-cyclohexyl benzene formamido group) phenyl] titanium.
(j) active ester compound:
As for the active ester compound (j) that is preferably used as radical initiator of the present invention, specifiable is the active sulphonic acid ester described in the imino group sulfonate compound described in the JP-B-62-6223 and JP-B-63-14340 and the JP-A-59-174831.
(k) contain the compound of carbon-halogen bond:
As for the compound that contains carbon-halogen bond (k) that is preferably used as radical initiator of the present invention, can be listed below the compound of molecular formula (6)～(12) representative.
Molecular formula (6)
In the molecular formula (6), X 2Represent halogen atom; Y 1Representative-C (X 2) 3,-NH 2,-NHR 38,-NR 38Or-OR 38Here, R 38Represent alkyl, substituted alkyl, aryl or substituted aryl.Equally, R 37Representative-C (X 2) 3, alkyl, substituted alkyl, aryl, substituted aryl or substituted alkenyl.
Molecular formula (7)
Figure G2004100070091D00462
In the molecular formula (7), R 39Represent alkyl, substituted alkyl, thiazolinyl, substituted alkenyl, aryl, substituted aryl, halogen atom, alkoxy, substituted alkoxy, nitro or cyano group; X 3Represent halogen atom; And n represents 1～3 integer.
Molecular formula (8)
Figure G2004100070091D00463
In the molecular formula (8), R 40Represent aryl or substituted aryl; R 41Represent any or halogen atom in the following group; Z 6Representative-C (=O)-,-C (=S)-or-SO 2-; X 3Represent halogen atom; M is 1 or 2.
Figure G2004100070091D00471
Here, R 42And R 43Represent alkyl separately, substituted alkyl, thiazolinyl, substituted alkenyl, aryl, perhaps substituted aryl; R 44And the R in the molecular formula (6) 38Identical.
Molecular formula (9)
In the molecular formula (9), R 45Optional aryl or the heterocyclic radical that replaces of representative; R 46Representative contains the tri haloalkyl or three haloalkenyl groups of 1～3 carbon atom; P is 1,2 or 3.
Molecular formula (10)
Figure G2004100070091D00473
Molecular formula (10) representative contains the carbonyl methylene heterogeneous ring compound of trihalomethyl group.L 7Represent hydrogen atom or molecular formula CO-(R 47) q(C (X 4) 3) rThe substituting group of representative; Q 2Represent sulphur atom, selenium atom, oxygen atom, dialkyl group methylene, alkene-1,2-subunit, 1,2-phenylene, perhaps N-R base; M 4That representative replaces or unsubstituted alkylidene or alkenylene, perhaps 1, the 2-arlydene; R 48Represent alkyl, aralkyl or alkoxyalkyl; R 47Represent carbocyclic ring or heterocycle divalence aromatic radical; X 4Represent the chlorine atom, bromine atoms or iodine atom; Q=0 and r=1, perhaps q=1 and r=1 or 2.
Molecular formula (11)
Figure G2004100070091D00481
Molecular formula (11) is represented 4-halo-5-(halogenated methyl-phenyl)-oxazole derivants.X 5Represent halogen atom; T represents 1～3 integer; S represents 1～4 integer; R 49Represent hydrogen atom or CH 3-tX 5 tBase; R 50Representing valence state is the unsaturated organic group of the optional replacement of s.
Molecular formula (12)
Molecular formula (12) is represented 2-(halogenated methyl-phenyl)-4-halo-oxazole derivants.X 6Represent halogen atom; V represents 1～3 integer; U represents 1～4 integer; R 51Represent hydrogen atom or CH 3-vX 6 vBase; R 52Representing valence state is the unsaturated organic group of the optional replacement of u.
The instantiation that contains the compound of carbon-halogen bond comprises the Bull.Chem.Soc.Japan of Wakabayashi etc., compound described in 42,2924 (1969), for example 2-phenyl-4, two (the trichloromethyl)-S-triazines of 6-, 2-(rubigan)-4, two (the trichloromethyl)-S-triazines of 6-, 2-(p-methylphenyl)-4, two (the trichloromethyl)-S-triazines of 6-, 2-(p-methoxyphenyl)-4, two (the trichloromethyl)-S-triazines of 6-, 2-(2 ', 4 '-dichlorophenyl)-4, two (the trichloromethyl)-S-triazines of 6-, 2,4,6-three (trichloromethyl)-S-triazine, 2-methyl-4, two (the trichloromethyl)-S-triazines of 6-, 2-n-nonyl-4, two (trichloromethyl)-S-triazines of 6-and 2-(α, α, β-three chloroethyl)-4, two (the trichloromethyl)-S-triazines of 6-.In addition, BrP 1,388, compound described in 492,2-styryl-4 for example, two (the trichloromethyl)-S-triazines of 6-, 2-(p-methylstyrene base)-4, two (the trichloromethyl)-S-triazines of 6-, 2-(to the methoxy styryl)-4, two (the trichloromethyl)-S-triazines of 6-and 2-(to the methoxy styryl)-4-amino-6-trichloromethyl-S-triazine; Compound described in the JP-A-53-133428,2-(4-methoxyl-naphtho--1-yl)-4 for example, 6-pair-trichloromethyl-S-triazine, 2-(4-ethoxy-naphtho--1-yl)-4,6-pair-trichloromethyl-S-triazine, 2-[4-(2-ethoxyethyl)-naphtho--1-yl]-4,6-pair-trichloromethyl-S-triazine, 2-(4,7-dimethoxy-naphtho--1-yl)-4,6-pair-trichloromethyl-S-triazine and 2-(acenaphtho-5-yl)-4,6-pair-trichloromethyl-S-triazine; And Deutsche Bundespatent 3,337, the compound described in 024, for example following compound.
Can also enumerate F.C.Schaefer etc. at J.Org.Chem., the compound of describing in 29,1527 (1964), for example 2-methyl-4, two (the trisbromomethyl)-S-triazines of 6-, 2,4,6-three (trisbromomethyl)-S-triazine, 2,4,6-three (two bromomethyls)-S-triazine, 2-amino-4-methyl-6-trisbromomethyl-S-triazine and 2-methoxyl-4-methyl-6-trichloromethyl-S-triazine.That can enumerate in addition, has the compound described in the JP-A-62-58241, a for example following compound.
In addition, can enumerate the compound described in the JP-A-5-281728, for example following compound.
Figure G2004100070091D00521
As selection, one group of compound that can be listed below, it is that those skilled in the art is according to M.P.Hutt, E.F.Elslager and L.M.Herbel are at Journal of Heterocyclic Chemistry, Vol.7 (No.3), 511 pages, and the synthetic at an easy rate compound of the synthetic method described in following or the like (1970).For example following compound:
(l) azo-based compound:
As for the azo-based compound that is preferably used as radical initiator of the present invention (1), can be listed below compound: 2,2 '-azobis isobutyronitrile, 2, the two propionitrile of 2 '-azo, 1,1 '-azo two (cyclohexanes-1-nitrile), 2,2 '-azo is two-(2-methylbutyronitrile), 2,2 '-azo is two-(2, the 4-methyl pentane nitrile), 2,2 '-azo is two-(4-methoxyl-2,4-methyl pentane nitrile), 4,4 '-azo two (4-cyanopentanoic acid), 2, the two isobutyric acid dimethyl esters of 2 '-azo, 2,2 '-azo two (2-methyl propanamide oxime), 2,2 '-azo-two [2-(2-imidazoline-2-yl) propane], 2,2 '-azo two (2-methyl-N-[1, two (the methylol)-2-hydroxyethyls of 1-] propionamide), 2,2 '-azo two [2-methyl-N-(2-hydroxyethyl) propionamide], 2,2 '-azo two (N-butyl-2-methyl propanamide), 2,2 '-azo two (N-cyclohexyl-2-methyl propanamide), 2,2 '-azo two [N-(2-propenyl)-2-methyl propanamide], and 2,2 '-azo two (2,4, the 4-trimethylpentane).
Among the present invention, can enumerate above-mentioned aromatic ketone (a), salt compound (b), organic peroxide (c), Hexaarylbiimidazole compound (e), Metallocenic compound (i) and contain the compound (k) of carbon-halogen bond is as the more preferably example of radical initiator.Wherein, can enumerate fragrant salt compounded of iodine, fragrant sulfonium salt, the trihalomethyl group-S-triazine of two cyclopentadiene titanium compounds and molecular formula (6) representative is as the most preferably example of radical initiator.The addition of radical initiator in polymerisable compound can account for 0.1～50% of polymerisable compound total solid weight, preferably accounts for 0.5～30%, is preferably 5～20% especially.
Among the present invention, radical initiator is fit to use separately or two or more mix use.
The compound of an alkene formula unsaturated link [(C) contain at least]
The compound (polymerizable compound) that contains an alkene formula unsaturated link at least that uses in the polymerisable compound of the present invention is selected from and contains an alkene formula unsaturated link at least, preferably contains the compound of two or more alkene formula unsaturated links.Such one group of compound is known in the art, and these compounds can use in the present invention without restriction.The chemical species of these compounds is, for example monomer or performed polymer, that is: dimer, tripolymer and oligomer, perhaps their potpourri or multipolymer.The example of monomer and multipolymer thereof is unsaturated carboxylic acid (for example acrylic acid, methacrylic acid, itaconic acid, crotonic acid, methacrylate and maleic acid) and ester and acid amides; The ester that forms between preferred unsaturated carboxylic acid and the aliphatic polyol compound, and the acid amides that forms between unsaturated carboxylic acid and the aliphatic polyamine compound.Can also suitably use and contain nucleophilic displacement of fluorine base (hydroxyl for example, amino and sulfydryl) esters of unsaturated carboxylic acids or the addition reaction product of acid amides and simple function group or many functional group isocyanates or epoxy, and and the dehydration condensation product of simple function group or polyfunctional group carboxylic acid.Equally, contain the esters of unsaturated carboxylic acids of close electric substituting group (for example isocyanate group and epoxy radicals) or the addition reaction product of acid amides and simple function group or multi-group alcohol, amine or mercaptan, and contain the esters of unsaturated carboxylic acids of elimination of group (for example halogeno-group and tosyloxy) or the displacement reaction product of acid amides and simple function group or multi-group alcohol, amine or mercaptan also is suitable.One group of compound that can also use above-mentioned carboxylic acid to be replaced by unsaturated sulfonic acid, styrene, vinyl ether etc.
The instantiation of the monomer of the ester of aliphatic polyol compound and unsaturated carboxylic acid is as follows.The example of acrylate comprises: glycol diacrylate, triethylene glycol diacrylate, 1, the 3-butanediol diacrylate, 1,4-butanediol diacrylate, propylene glycol diacrylate, neopentylglycol diacrylate, trimethylolpropane triacrylate, trimethylolpropane tris (acryloyl-oxy propyl group) ether, trimethylolethane trimethacrylate acrylate, hexanediyl ester, 1,4-cyclohexanediol diacrylate, tetraethylene glycol diacrylate, pentaerythritol diacrylate, pentaerythritol triacrylate, tetramethylol methane tetraacrylate, dipentaerythritol diacrylate, dipentaerythritol acrylate, the D-sorbite triacrylate, D-sorbite tetraacrylate, D-sorbite five acrylate, D-sorbite six acrylate, three (acrylyl oxy-ethyl) chlorinated isocyanurates and acrylic polyester oligomer.
The example of methacrylate comprises: 1, the 4-butanediol dimethylacrylate, triethylene glycol dimethacrylate, neopentylglycol dimethacrylate, trimethylol-propane trimethacrylate, the trimethylolethane trimethacrylate methacrylate, ethylene glycol dimethacrylate, the 1,3 butylene glycol dimethylacrylate, hexanediol dimethacrylate, dimethyl pentaerythritol acrylate, pentaerythritol acrylate trimethyl, pentaerythrite tetramethyl acrylate, the dipentaerythritol dimethylacrylate, dipentaerythritol hexamethyl acrylate, D-sorbite trimethyl acrylic ester, D-sorbite tetramethyl acrylate, two [right-(3-methacryloxy-2-hydroxyl propoxyl group) phenyl] dimethylmethane, and two [right-(methacryloxypropyl ethoxy) phenyl] dimethylmethane.
The example of itaconate comprises the ethylene glycol bisthioglycolate itaconate, the propylene glycol diitaconate, 1,3-butylene glycol diitaconate, 1,4-butylene glycol diitaconate, 1,4-butylene glycol diitaconate, pentaerythrite diitaconate and D-sorbite four itaconates. the example of crotonates comprises the ethylene glycol bisthioglycolate crotonates, 1,4-butylene glycol two crotonatess, pentaerythrite two crotonatess and D-sorbite four crotonatess. the example of methacrylate comprises glycol ester diisobutylene, pentaerythrite diisobutylene acid esters and D-sorbite tetra methylacrylate. the example of maleate comprises the ethylene glycol bisthioglycolate maleate, triethylene glycol dimaleate, pentaerythrite dimaleate and D-sorbite four maleates.
As for other example of ester, also be fit to use JP-B-46-27926, the fatty alcohol radical ester described in JP-B-51-47334 and the JP-A-57-196231, JP-A-59-5240, the ester that contains the aryl skeleton described in JP-A-59-5241 and the JP-A-2-226149; And the ester that contains amino described in the JP-A-1-165613.Can use the potpourri of above-mentioned ester monomer in addition.
The example of the amide monomer that forms between aliphatic polyamine compound and the unsaturated carboxylic acid comprises: methylene-bisacrylamide, the di-2-ethylhexylphosphine oxide Methacrylamide, 1,6-hexylidene bisacrylamide, 1, the two Methacrylamides of 6-hexylidene, diethylene triamine three acrylamides, the two Methacrylamides of inferior dimethylbenzene bisacrylamide and inferior dimethylbenzene.As for other preferred embodiment, can enumerate and have the compound described in the JP-B-54-21726 with cyclohexylidene structure based on the monomer of acid amides.
Equally, the urethane ester group addition polymerizable compound by the addition reaction manufacturing between isocyanates and the hydroxyl also is suitable for.As instantiation, that enumerates has: contain the vinyl urethane compounds of two or more polymerizable vinyl in the per molecule described in JP-B-48-41708, this compound is to be added in the polyisocyanate compounds that contains two or more isocyanate group in the per molecule by the hydroxyl vinyl monomer with following molecular formula representative to prepare.
CH 2＝C(R 4)COOCH 2CH(R 5)OH
R in the molecular formula 4And R 5Represent H or CH separately 3
Urethanes acrylate described in JP-A-51-37193, JP-B-2-32293 and the JP-B-2-16765; And the urethane compounds described in JP-B-58-49860, JP-B-56-17654, JP-B-62-39417 and the JP-B-62-39418 with Oxyranyle skeleton.In addition, use the polymerizable compound that contains amino structure or sulfide based structural in the molecule described in JP-A-63-277653, JP-A-63-260909 and the JP-A-1-105238, the polymerizable compound that can obtain to have very excellent film speed.
Other example comprises polyester acrylate, and by epoxy resin multi-functional acrylate or (methyl) acrylate with the epoxy acrylate of (methyl) acrylic acid reaction acquisition, described as JP-A-48-64183, JP-B-49-43191 and JP-B-52-30490.Also can enumerate JP-B-46-43946, the special unsaturated compound described in JP-B-1-40337 and the JP-B-1-40336; And the compound described in the JP-A-2-25493 based on vinyl phosphonate.In some cases, also be fit to use the compound that contains the perfluoroalkyl structure that has described in the JP-A-61-22048.In addition, that can also use is Journal of The AdhesiveAssociation of Japan, Vol.20, the compound of introducing among the No.7,300-308 page or leaf (1984) as photocurable monomer or oligomer.
Details about these polymerizable compound using method, the structure that comprises them, be used singly or in combination, and addition, can set up arbitrarily according to its purposes, for example when using polymerisable compound of the present invention as Lighographic printing plate precursor, performance design according to final Lighographic printing plate precursor is determined using method. for example, select according to following viewpoint. consider from film speed position, the high structure of unsaturated group content in the preferred molecule, preferred in many cases difunctional or polyfunctional compound. also have, in order to improve image area, promptly solidify film strength, preferred three palaces can be rolled into a ball or polyfunctional compound. and, by being used in combination the compound that contains different functional groups and different polymerizable group (acrylate for example, methacrylate, compound of styryl and vinyl ether compound), although and the method for regulating film speed and film strength simultaneously also is effective. the compound of high-molecular weight compounds or high hydrophobicity has excellent film speed and film strength, but consider possibility and improper from developing powder and the deposition viewpoint developer solution. same, as for recording layer in other component (binder polymer for example, initiating agent and colorant) affinity or the dispersiveness in them, but the selection of polyaddition compounds and using method are important factors. for example, can strengthen affinity by using the low-purity compound or being used in combination two or more compounds. also have, for improve with base material or and the clinging power of the external coating described after a while, can select a kind of special construction. as for the proportion scale of polymerizable compound in the recording layer, consider that from the sensitivity viewpoint high charge ratio is favourable. when charge ratio is too high, undesirable being separated may appear, may cause problem in the manufacturing step (for example transfer of recording layer component and the manufacturing failure that causes by adhesiveness) owing to the viscosity of recording layer, also may cause such as the problem that in developer solution, precipitates. consider from these viewpoints, the consumption of preferred polymerizable compound accounts for 5～80% of nonvolatile element weight in the polymerisable compound, more preferably 25～75%. these polymerizable compounds can use separately or two or more mixing uses. in addition, using method as for polymerizable compound, suitable construction, charge ratio and addition, can be according to polymerization inhibition degree to oxygen, resolution, the painted phase of mist formation, the change of refraction coefficient, surface adhesives etc. are selected arbitrarily. but also can carry out the structure or the coating process of layer as required, for example primary coat and being coated with outward.
[(D) infrared absorbent]
Polymerisable compound of the present invention is characterised in that to comprise and absorbs infrared ray and they are changed into the infrared absorbent of heat energy.By exposing, thereby quicken the free radical reaction of formation of radical initiator and the polyreaction of polymerizable compound with light with wavelength that infrared absorbent can absorb.As for such infrared absorbent, enumerate be known spectral sensitization dyestuff or dyestuff or absorbing light and and the optical free radical initiating agent interactional pigment is arranged.
＜spectral sensitization dyestuff or dyestuff 〉
The spectral sensitization dyestuff that the present invention uses or the preferred embodiment of dyestuff comprise fragrant multinuclear (for example pyrene perylene and benzo [9,10] phenanthrene), xanthene class (fluorescein for example, eosin, erythromycin, rhodamine B and rose-red), cyanine class (for example the sulfo-carbocyanine is with the Evil carbocyanine), merocyanine class (for example merocyanine and carbonyl merocyanine), thiazide (for example thionine, methylenum careuleum and toluidine blue), acridine (acridine orange for example, chloroflavin and acriflavine), phthalocyanines (for example phthalocyanine and metal-phthalocyanine), porphyrin class (for example porphyrin of tetraphenylporphyrin and central metal replacement), chlorophyll class (chlorophyll for example, the chlorophyll that chlorophyllin and central metal replace), metal complex, anthraquinone class (for example anthraquinone), side's class (for example side), and following compound.
Figure G2004100070091D00571
As for preferred spectral sensitization dyestuff or dyestuff, the compound that can enumerate has: the pyralium salt of describing among the JP-B-40-28499, and for example following compound:
Figure G2004100070091D00581
Cyanine described in the JP-B-46-42363, for example following compound:
Coumarone dyestuff described in the JP-A-2-63053, for example following compound:
Conjugation ketone dyes described in JP-A-2-85858 and the JP-A-2-216154, for example following compound:
Azo cinnamylidene derivant described in dyestuff described in the JP-A-57-10605 and the JP-B-2-30321, for example following compound:
Cyanine radical dye described in the JP-A-1-287105, for example following compound:
Xanthyl dyestuff described in JP-A-62-31844, JP-A-62-31848 and the JP-A-62-143043, for example following compound:
And the aminobenzene vinyl ketone described in the JP-B-59-28325, for example following compound:
Figure G2004100070091D00621
Following infrared absorbent (dyestuff or pigment) also is to be especially suitable for use as sensitizing dyestuff.The preferred embodiment of these dyestuffs comprises JP-A-58-125246, JP-A-59-84356, the cyanine dye described in JP-A-59-202829 and the JP-A-60-78787; With the cyanine dye described in the BrP 434,875.
In addition, can be suitable for cyanine dye example of the present invention and comprise [0017]～[0019] section of the cyanine dye described in the following file: JP-A-2001-133969, [0012] of JP-A-2002-40638～[0038] section, and JP-A-2002-23360 [0012]～[0023] section.Instantiation comprises following illustrational compound.
U.S.P 5,156, and the near infrared absorption sensitizer described in 938 also is to be fit to use.In addition, U.S.P3, substituted aryl benzo (sulfo-) pyralium salt described in 881,924; Cyclonite thiophene pyralium salt described in the JP-A-57-142645 (U.S.P4,327,169); JP-A-58-181051, JP-A-58-220143, JP-A-59-41363, JP-A-59-84248, JP-A-59-84249, the pyranylation compound described in JP-A-59-146063 and the JP-A-59-146061; Cyanine dye described in the JP-A-59-216146; U.S.P 4,283, five methine sulfo-pyralium salts described in 475; And the pyrylium compound described in JP-B-5-13514 and the JP-B-5-19702 also is preferred the use.
Can also enumerate U.S.P 4,756, molecular formula described in 993 (I) and hear-infrared absorption dye (II), and the phthalocyanine radical dye described in the EP916513A2 is as preferred dyestuff.
In addition, the negative ion infrared absorbent described in the Japanese patent application 10-79912 also is to be fit to use.The negative ion infrared absorbent of herein mentioning is meant that the ultrared dyestuff matrix of main absorption does not have cationic structural, but has the sort of infrared absorbent of anion structure.The example comprises (a) negative ion metal complex, (b) negative ion carbon black, (c) negative ion phthalocyanine, and (d) compound of following molecular formula (21) representative.The counterion of these negative ion infrared absorbents is monovalent cation or the multivalent cations that contain proton.
Molecular formula (21)
(21)
[G 9-M 5-G 10] m (X 10) +
The negative ion metal complex of herein mentioning (a) is meant that central metal in the main light absorbing complex part and part are whole becomes an anionic compound.
As for negative ion carbon black (b), what enumerate is with anion base, and for example sulfonic group and carboxylic acid group are the substituent carbon black of combination.In order on carbon black, to introduce this group, can adopt Carbon BlackHandbook, the above method of 12 pages of the third editions (The Carbon Black Association edits, and The Carbon BlackAssociation publishes on April nineteen ninety-five 5) with the specified acid oxidized black.Negative ion phthalocyanine (c) refers on phthalocyanine frame and is combined as substituting group in conjunction with the negative ion in above-mentioned (b), and makes whole molecule become anionic phthalocyanine.
To describe the compound (d) of above-mentioned molecular formula (21) representative below in detail.In the molecular formula (21), G 9Represent anion substituent; G 10Substituent in the representative; (X 10) +Representing valence state is the kation that contains proton of 1～m; M represents 1～6 integer; M 5Represent conjugated chain.This conjugated chain M 5Substituting group can be arranged or have ring texture.Conjugated chain M 5Can represent with following molecular formula.
In the molecular formula, R 80, R 81And R 82Represent hydrogen atom independently of one another, halogen atom, cyano group, alkyl, aryl, thiazolinyl, alkynyl, carbonyl, thio group, sulfonyl, sulfinyl, the oxygen base, perhaps amino;
R 80, R 81And R 82Can be combined together to form ring structure; N represents 1～8 integer.
In the negative ion infrared absorbent of molecular formula (21) representative, preferably use following IRA-1～IRA-5.
Also can preferably use the kation infrared absorbent of following IRC-1～IRC-44 representative.
Figure G2004100070091D00741
Figure G2004100070091D00781
In the said structure formula, T -Represent the monovalence balance anion, be preferably halide anion (F for example -, Cl -, Br -And I -), Lewis acid anion (BF for example 4 -, SbCl 6 -And ClO 4 -), alkyl sulfonic acid negative ion, perhaps aryl sulfonic acid negative ion.
Term in the abovementioned alkyl sulfonic acid " alkyl " refers to the linearity that contains 1～20 carbon atom, branching or cyclic alkyl. instantiation comprises: methyl, ethyl, propyl group, butyl, amyl group, hexyl, heptyl, octyl group, nonyl, decyl, undecyl, dodecyl, tridecyl, cetyl, octadecyl, eicosyl, isopropyl, isobutyl, sec-butyl, the tert-butyl group, isopentyl, neopentyl, 1-methyl butyl, isohesyl, the 2-ethylhexyl, 2-methyl hexyl, cyclohexyl, cyclopentyl and 2-norborny. wherein more preferably contain the linear alkyl of 1～12 carbon atom, contain the branched-alkyl of 3～12 carbon atoms, contain the naphthenic base of 5～10 carbon atoms.
The condensed ring that term in the above-mentioned aryl sulfonic acid " aryl " refers to the group that formed by a phenyl ring, formed by two or three phenyl ring, the perhaps condensed ring that forms by the unsaturated ring of phenyl ring and 5-unit.Instantiation comprises: phenyl, naphthyl, anthryl, phenanthryl, indenyl, acenaphthenyl and fluorenyl.Wherein more preferably phenyl and naphthyl.
Can also preferably use the nonionic infrared absorbent of following IRN-1～IRN-9 representative.
Figure G2004100070091D00811
In the compound that exemplifies above, preferred especially respectively IRA-1 is as the negative ion infrared absorbent; Preferred especially IRC-7, IRC-30, IRC-40 and IRC-42 are as the kation infrared absorbent; Preferred especially IRN-9 is as the nonionic infrared absorbent.
＜pigment 〉
As for can be used for pigment of the present invention, specifiable have the pigment described in commercially available pigment and the following document: Color Index (C.I.) Handbook; Saishin Ganryo Binran (Current PigmentHandbook), Nippon Ganryo Pigment Kyokai edits (1977); Saishin Ganryo OhyoGijutsu (Current Pigment Application Technologies), CMC Publishing Co., Ltd. publishes (1986); And Insatsu Inki Gijutsu (Printing Ink Technologies), CMCPublishing Co., Ltd. publishes (1984).
The example of pigment comprises: mineral black, yellow pigment, orange pigment, brown pigment, red, purple dye, blue pigment, green pigment, fluorescent pigment, metal powder pigment and other polymkeric substance-bonding dyestuff.Instantiation comprises: insoluble AZO pigments, azo lake pigment, condensed azo pigment, chelating AZO pigments, phthalocyanine base pigment, anthraquinonyl pigment ， perylene base pigment, perinone base pigment, thioindigo base pigment, quinoline a word used for translation (two) ketone group pigment ， dioxazine base pigment, isoindoline ketone group pigment, quinophthalones base pigment, dyeing mordant pigment, azine pigment, nitroso pigments, nitropigments, natural pigment, fluorescent pigment, inorganic pigment and carbon black.In these pigment, carbon black preferably.
It can be not surface treated or surface treated can be used for pigment of the present invention.As for surface treatment method, can consider following method: coat the method for resin or wax on the surface, the method for adhesive surface activating agent, and on surface of pigments the method (for example silane coupling reagent, epoxy compound and polyisocyanate) of coupled reaction thing.These methods are described in the following document: Kinzoku Sekken NoSeishitsu To Ohyo (Properties and Applications of Metallic Soaps), and Saiwai Shobo publishes; Insatsu Inki Gijutsu (Printing Ink Technologies), CMC Publishing Co., Ltd. publishes (1984); And Saishin Ganryo Ohyo Gijutsu (Current Pigment ApplicationTechnologies), CMC Publishing Co., Ltd. publishes (1986).
The grain size of pigment is preferably 0.01 μ m～10 μ m, and more preferably 0.05～1 μ m is preferably 0.1～1 μ m especially.When granules of pigments size less than 0.01 μ m, consider it is not preferred from the dispersion stabilization angle of pigment the image recording layer masking liquid.On the other hand, consider that from the homogeneity angle of image recording layer the pigment that surpasses 10 μ m also is not preferred.
As for the method for dispersed color, can adopt the known dispersion technology that when making ink or making toner, uses.The example of dispersion machine comprises: ultrasonic dispersing machine, sand mill, attitor, ball mill, super grinding machine, bowl mill, homo-mixer, fan diffuser, KD grinding machine, rubber mill, dynatron (dynatron), three-roll mill and pressure kneading machine.Detail is described in Saishin Ganryo Ohyo Gijutsu's in (Current Pigment Application Technologies), CMC Publishing Co., and Ltd. (1986) publishes.
Additional disclosure once, although purpose is the infrared absorbent that quickens polymerisable compound curing reaction of the present invention and can directly joins in the composition together with other component, but place provides another layer at contiguous said composition layer, adds infrared absorbent and also can obtain identical effect in this adjacent layer.
Particularly, when as described later, when using polymerisable compound of the present invention, infrared absorbent can be added to image recording material with in one deck, perhaps be added in another layer as the negative type image recording material of Lighographic printing plate precursor.But when preparation negative type image recording material, preferred recording layer is in 300nm～1, and the optical density of maximum absorption wave strong point is 0.1～3.0 in the 200nm scope.When optical density exceeds this scope, easy desensitization.Owing to optical density is to be determined by the addition of sensitizing dyestuff and the thickness of recording layer, can be by controlling the optical density that these two conditions obtain appointment.The optical density of recording layer can be measured with customary way.The example of measuring method comprises following method: form recording layer on transparent or white support, the thickness of recording layer has been defined in the suitable scope, make the dried amount of being coated with meet the requirement of lithographic plate, measure the method for its optical density then with transmission-type light densitometer; And on reflection carrier, form recording layer such as aluminium, measure the method for its reflection density again.
[(E) binder polymer]
In order to improve membrane property, in polymerisable compound of the present invention, can use (E) binder polymer as required.The linear organic polymer of preferred use is as binder polymer.As for this " linear organic polymer ", can use any known linear organic polymer arbitrarily.Develop in order to carry out water development or alkalescent water, preferably can dissolve in water or in the alkalescent water or the linear organic polymer of swelling.Select and use the purpose of linear organic polymer to be not only film forming agent according to the application as image recording material, and as water, alkalescent water or organic solvent developer.For example, when using water-soluble organic polymer, can carry out water development.The example of this linear organic polymer comprises the free radical polyalcohol that has the carboxylic acid group in the side chain, as JP-A-59-44615, and JP-B-54-34327, JP-B-58-12577, JP-B-54-25957, JP-B-54-92723, the free radical polyalcohol described in JP-A-59-53836 and the JP-A-59-71048, that is: methacrylic acid copolymer, acrylic copolymer, itaconic acid copolymer, crotonic acid multipolymer, maleic acid, the maleic acid of partial esterification etc.Also can enumerate the acid cellulose derivant that side chain contains the carboxylic acid group.In addition, can also use the polymkeric substance of the hydroxyl that has added cyclic acid anhydride.
Particularly, contain (methyl) acryl resin and the double bond containing alkaline bleach liquor soluble resin of side chain that carboxyl is arranged on benzyl or allyl and the side chain, as JP-A-2000-187322, JP-A-2002-62648, Japanese patent application 2001-253217 and 2002-287920, with the resin described in the JP-A-2002-62648, owing to being applicable to the present invention in the balance that has excellence aspect film strength, sensitivity and the development.
Equally, JP-B-7-12004, JP-B-7-120041, JP-B-7-120042, JP-B-8-12424, JP-A-63-287944, JP-A-63-287947, the urethanes based adhesive polymkeric substance that contains acidic group described in JP-A-1-271714 and the Japanese patent application 10-116232 is very excellent aspect intensity, thereby considers it is favourable from the adaptive printability resistance angle of low exposure.
In addition, can use polyvinylpyrrolidone and polyethylene oxide water-soluble linear organic polymer as other.In order to increase the curing film strength, can also use alcohol soluble nylon and 2, the polyester that forms between 2-pair-(4-hydroxyphenyl)-propane and the chloropropylene oxide.
As for being used for polymkeric substance of the present invention, preferably its weight-average molecular weight is more than or equal to 5,000, and more preferably 10,000～300,000; Preferred its number-average molecular weight is more than or equal to 1,000, and more preferably 2,000～250,000.Preferred its polydispersity (weight-average molecular weight/number-average molecular weight) is more than or equal to 1, and more preferably 1.1～10.
Although these polymkeric substance can be any in atactic polymers, block polymer or the graft polymer, be preferably atactic polymers.
Can adopt known conventional method to synthesize and be used for polymkeric substance of the present invention.The example of synthetic solvent for use comprises: tetrahydrofuran, 1,2-ethylene dichloride, cyclohexanone, methyl ethyl ketone, acetone, methyl alcohol, ethanol, the ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, acetate (2-methoxyethyl) ester, diethylene glycol dimethyl ether, 1-methoxyl-2-propyl alcohol, acetate (1-methoxyl-2-propyl group) ester, N, dinethylformamide, N,N-dimethylacetamide, toluene, ethyl acetate, methyl lactate, ethyl lactate, dimethyl sulfoxide and water.These solvents can use separately or two or more mix use.
Example at the synthetic radical polymerization initiator that uses when being used for polymkeric substance of the present invention comprises compound known, for example azo group initiating agent and peroxide initiator.
In the present invention, binder polymer can use separately or two or more mix to use. when using polymerisable compound of the present invention as the image recording material of Lighographic printing plate precursor, the addition of binder polymer accounts for 20～95% of image recording material total weight of solids, preferably account for 30～90%. when binder polymer addition less than 20 weight %, insufficient when forming image to the enhancing effect of image area intensity. on the other hand, when addition surpasses 95 weight %, can't form image. also preferably contain the compound of an alkene formula unsaturated link at least and the weight ratio of linear organic polymer is 1/9～7/3.
The polymerisable compound of the present invention of Huo Deing has excellent sensitivity and storage stability like this, is especially suitable for use as the image recording material of negative planographic printing plate precursor.
[application in Lighographic printing plate precursor]
When using polymerisable compound of the present invention as the image recording material of Lighographic printing plate precursor, polymerisable compound can be dissolved in the solvent and this solution is coated on the suitable carriers, produce image recording material.And, other layer that can also form adjuvant, back coating, interlayer, protective seam and describe after a while according to purpose.
Can in polymerisable compound of the present invention, use the dyestuff of the dyestuff of big absorption as image arranged at visible region.Instantiation comprises: oil yellow #101, oil yellow #103, the red #312 of oil-bound distemper, glossy dark green BG, oil blue BOS, oil blue #603, glossy black BY, glossy black BS and glossy black T-505 (these all are by Orient ChemicalIndustries, and Ltd. makes), Victoria's ethereal blue, crystal violet (CI42555), methyl violet (C142535), ethyl violet, rhodamine B (CI145170B), malachite green (CI42000), the dyestuff described in methylene blue (CI52015) and the JP-A-62-293247.Pigment such as phthalocyanine base pigment, azo group pigment, carbon black and titania also is to be fit to use.
Preferred add so a kind of colorant, because like this after image forms, differentiate between images district and non-image district easily.Additional disclosure once, the addition of colorant accounts for 0.01～10% of total weight of solids in the recording layer masking liquid.
Equally, in the present invention,, need to add a spot of thermal polymerization inhibitor in order to prevent that unnecessary thermal polymerization appears in polymerizable compound in polymerisable compound preparation or the storage process.Suitable thermal polymerization inhibitor example comprises quinhydrones, p methoxy phenol, two-tert-butyl group-p-Cresol, pyrogallol, tert-butyl catechol, benzoquinones, 4,4 '-thiobis (3 methy 6 tert butyl phenol), 2,2 '-di-2-ethylhexylphosphine oxide (4-methyl-6-tert butyl phenol), and N-nitroso--N-Phenylhydroxylamine aluminium salt.The addition of thermal polymerization inhibitor accounts for about 0.01～about 5% of total composition weight.If desired, the polymerization inhibiting effect for anti-block can also add advanced higher fatty acid derivative, and for example mountain Yu acid and mountain Yu acid amides make in their drying steps after being coated with to be present on the recording layer surface.The addition of preferred advanced higher fatty acid derivative accounts for about 0.1%～about 10% of composition total weight.
Equally, polymerisable compound of the present invention is mainly used in the recording layer that forms Lighographic printing plate precursor.In order to widen the Treatment Stability of this recording layer, can add the amphoteric surfactant described in the non-ionic surfactant described in JP-A-62-251740 and the JP-A-3-208514 and JP-A-59-121044 and the JP-A-4-13149 to development conditions.
The instantiation of non-ionic surfactant comprises: sorbitan tristearate, sorbitan monopalmitate, sorbitan trioleate, monostearin, and polyoxyethylene nonylplenyl ether.
Examples of amphoteric surfactants comprises: alkyl two (amino-ethyl) glycocoll, alkyl gathers the amino-ethyl glycine hydrochloride, 2-alkyl-N-carboxyethyl N-hydroxyethyl imidazole betaine, and N-myristyl-N, N-betaine type (for example Amorgen K (trade name) of Daiichi Kogyo K.K. manufacturing).
Non-ionic surfactant or the amphoteric surfactant ratio in the recording layer masking liquid is preferably 0.05～15 weight %, more preferably 0.1～5 weight %.
In addition, have pliability etc., can in recording layer masking liquid of the present invention, add plastifier as required in order to make to film.The example comprises: polyglycol, tributyl citrate, diethyl phthalate, dibutyl phthalate, dihexylphthalate, dioctyl phthalate, tricresyl phosphate (toluene ester), tributyl phosphate, trioctyl phosphate, and tetrahydrofurfuryl oleate.
When using polymerisable compound of the present invention to make Lighographic printing plate precursor, usually can be dissolved in component and each essential component of masking liquid of polymerisable compound in the solvent together, subsequently this solution being coated on the suitable carriers. the examples of solvents of Shi Yonging comprises herein: 1, the 2-ethylene dichloride, cyclohexanone, methyl ethyl ketone, acetone, methyl alcohol, ethanol, propyl alcohol, the ethylene glycol monomethyl ether, 1-methoxyl-2-propyl alcohol, acetate (2-methoxyethyl) ester, dimethoxy ethane, methyl lactate, ethyl lactate, N,N-dimethylacetamide, N, dinethylformamide, tetramethylurea, N-Methyl pyrrolidone, dimethyl sulfoxide, sulfolane, gamma-butyrolacton, toluene and water. but should be appreciated that the present invention is not limited to this. these solvents can use or mix use separately. and the concentration of said components (all solids that comprises adjuvant) in solvent is preferably 1～50 weight %.
Can also change the dried amount of being coated with of recording layer (solids content) that is coated on the carrier according to practical situations, but when being used for Lighographic printing plate precursor, be preferably 0.5～5.0g/m usually 2When the amount of being coated with reduced, although apparent sensitivity has improved, the membrane property of recording layer descended.
Can adopt the whole bag of tricks as coating process.The example comprises: rod is coated with machine and is coated with method, spin-coating method, and spraying process, the curtain coating method, dip coating, the air-knife coating method, scraper is coated with method and rolling method.
Can add surfactant in recording layer masking liquid of the present invention, for example the fluorine based surfactant described in the JP-A-62-170950 applies character to improve.The addition of this surfactant preferably accounts for 0.01～1% of recording layer total solids content, more preferably 0.05～0.5 weight %.
(carrier)
As for carrier used when using polymerisable compound of the present invention to make the offset printing plate precursor, can use the stable board-like material of size, and have no particular limits.The example comprises paper, lamination the paper of plastics (for example tygon, polypropylene and polystyrene), sheet metal (for example aluminium, zinc and copper), and plastic foil (cellulose diacetate for example, cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate-butyrate, cellulose nitrate, polyethylene terephthalate, tygon, polystyrene, polypropylene, polycarbonate and Pioloform, polyvinyl acetal).These resin moldings or sheet metal can be to be made by independent material, or are made by two or more materials.The example comprised lamination or vapor deposition the paper or the plastic foil of above-mentioned metal, the perhaps laminate of different plastic foils.
Preferred polyester film or the aluminium sheet of using is as carrier.Wherein especially preferably have good dimensional stability and relatively cheap aluminium sheet.Suitable aluminium sheet be pure aluminum plate and be key component with aluminium, contain the alloy sheets of trace extraneous element, in addition, the plastic foil of aluminium that also can adopt lamination or vapor deposition.The example of contained extraneous element comprises in the aluminium alloy: silicon, iron, manganese, copper, magnesium, chromium, zinc, bismuth, nickel and titanium.The content of extraneous element in alloy is up to 10 weight %.Among the present invention, fine aluminium is particularly suitable.But pure aluminium is difficult on refining techniques owing to make fully, can use the aluminium that contains micro-extraneous element.To being used for aluminium sheet of the present invention, can suitably use known so far and already used aluminium sheet not stipulating aspect its composition.
The thickness of aluminium sheet is about 0.1～0.6mm, is preferably 0.15～0.4mm, is preferably 0.2～0.3mm especially.Before aluminium sheet is carried out coarse processing, if desired, aluminium sheet is carried out ungrease treatment, to remove lip-deep rolling oil with for example surfactant, organic solvent or alkaline aqueous solution.
Can adopt the whole bag of tricks that surface of aluminum plate is carried out coarse processing, mechanical surface roughening method for example, the method for electrochemical dissolution and rough surface, and the method on chemo-selective dissolving surface.As for mechanical means, can adopt known method, for example ball polishing, brush polishing, air blast polishing and moccasin polishing method.As for the electrochemical roughening method, can adopt and in hydrochloric acid or nitric acid electrolytic solution, use alternating current or galvanic method.Also disclosed two kinds of methods among the JP-A-54-63902 can be used in combination.
If desired, can carry out alkaline etching processing, neutralisation treatment to coarse like this aluminium sheet, carry out anodized again, to improve the water-retaining property or the wearing quality on surface. as for the electrolytic solution that is used for the aluminium sheet anodized, can use the various electrolytic solution that can form porous oxide film. generally can use sulfuric acid, phosphoric acid, oxalic acid, chromic acid or their acid mixture. concentration of electrolyte is suitably to determine according to the kind of electrolytic solution.
Anodised treatment conditions change according to electrolytic solution, therefore can not clearly stipulate.The general condition that is fit to is: electrolyte concentration is 1～80 weight %, and fluid temperature is 5～70 ℃, and current density is 5～60A/dm 2, voltage is 1～100V, electrolysis time is 10 seconds～5 minutes.
The quantity of preferred anodes oxide film is more than or equal to 1.0g/m 2, 2.0～6.0g/m more preferably 2Lazy weight 1.0g/m when anode oxide film 2The time, make the printability resistance deficiency easily, perhaps form wearing and tearing in the non-image district of lithographic plate easily, form so-called " wearing and tearing stain " phenomenon thereby in printing process, produce ink easily attached to fray.
Additional disclosure once, anodized is to carry out on the surface that will print of lithographic printing plate support.But,, generally also form 0.01～3g/m overleaf owing to be distributed to the back side of line of electric force 2Anode oxide film.
After anodized, adopt conventional known treatment method that carrier surface is carried out hydrophilic treatment.The method that hydrophilic treatment adopts is U.S.P 2,714, the method for disclosed use alkali silicate (for example sodium silicate aqueous solution) in 066,3,181,461,3,280,734 and 3,902,734.According to this method, carrier is carried out immersion treatment or electrolytic treatments with sodium silicate aqueous solution.In addition, can also adopt among the JP-B-36-22063 disclosed polyvinylphosphonic acid disposal route among disclosed potassium fluorozirconate disposal route and the U.S.P 3,276,868,4,153,461 and 4,689,272.
Wherein, the particularly preferred hydrophilic treatment method of the present invention is that silicate is handled.Below the silicate disposal route will be described.
The anode oxide film of the aluminium sheet handled like this is immersed in to contain 0.1～30 weight %, preferred 0.5～10 weight % alkali silicate, pH be in 10～13,25 ℃ the aqueous solution, for example handled 0.5～120 second down at 15～80 ℃.When the pH of alkali metal silicate aqueous solution is lower than 10, solution meeting gelling, and when pH was higher than 13.0, oxide film can dissolve.Being used for alkali silicate example of the present invention comprises: sodium silicate, potassium silicate and lithium metasilicate.The example that is used to increase the oxyhydroxide of alkali metal silicate aqueous solution pH comprises: NaOH, potassium hydroxide and lithium hydroxide.Additional disclosure once, treating fluid can with alkali salt or the compound use of IVB family slaine.The example of alkali salt comprises: water soluble salt, and as nitrate (for example calcium nitrate, strontium nitrate, magnesium nitrate and barium nitrate), sulfate, hydrochloride, phosphate, acetate, oxalates and borate.The example of IVB family slaine comprises: titanium tetrachloride, titanium trichloride, titanium potassium fluoride, titanium potassium oxalate, titanium sulfate, titanium tetra iodide, zirconium chloride oxide, zirconium dioxide, basic zirconium chloride and zirconium chloride.
These alkali salts or IVB family slaine can use separately or two or more are used in combination.The addition of slaine is preferably 0.01～10 weight %, more preferably 0.05～5.0 weight %.
Because silicate is handled the water wettability further improved surface of aluminum plate, ink in printing process hardly attached to non-image district, thereby improved anti-fouling performance.
(back coating)
Provide back coating at the carrier back side as required.As for this back coating, the preferred coating of making by the organic high molecular compound described in the JP-A-5-45885 of using, the perhaps coating of making by the metal oxide of organic or inorganic metallic compound hydrolysis described in the JP-A-6-35174 or polycondensation acquisition.
About these coatings, the alkyl oxide of silicon, for example Si (OCH 3) 4, Si (OC 2H 5) 4, Si (OC 3H 7) 4And Si (OC 4H 9) 4, cheaply and easily buying, the coating of using the metal oxide that obtains from the alkyl oxide of this silicon to make has excellent anti-development, thereby is particularly preferred.
(interlayer)
In Lighographic printing plate precursor of the present invention, interlayer can be arranged, its objective is the adhesiveness or the stain resistance that improve between recording layer and the base material.The instantiation of interlayer comprises the interlayer described in the following document:
JP-B-50-7481, JP-A-54-72104, JP-A-59-101651, JP-A-60-149491, JP-A-60-232998, JP-A-3-56177, JP-A-4-282637, JP-A-5-16558, JP-A-5-246171, JP-A-7-159983, JP-A-7-314937, JP-A-8-202025, JP-A-8-320551, JP-A-9-34104, JP-A-9-236911, JP-A-9-269593, JP-A-10-69092, JP-A-10-115931, JP-A-10-161317, JP-A-10-260536, JP-A-10-282682, JP-A-11-84674 and Japanese patent application 8-225335,8-270098,9-195863, JP-A-9-195864, JP-A-9-89646,9-106068,9-183834,9-264311,9-127232,9-245419,10-127602,10-170202,11-36377,11-165861,11-284091 and 2000-14697.
(protective seam)
In the Lighographic printing plate precursor of the present invention, owing to normally in air, expose, layer protective layer can also be provided on recording layer.Protective seam has prevented to enter in the recording layer such as the micromolecular compound of oxygen and alkaline matter, and these micromolecular compounds are present in airborne, suppresses easily to form reaction by the image that the recording layer exposure causes, thereby can expose in air.Therefore, claimed layer has following characteristic: the micromolecular compound such as oxygen is had low-permeability; Basically do not suppress the transmission of the light that is used to expose; With recording layer excellent adhesiveness is arranged; Remove easily in the development step after exposure.About this protective seam, made plurality of devices up to now, detail is described in U.S.P3,458,311 and JP-A-55-49729 in.As for the material that can be used as protective seam, can use excellent relatively crystalline water-soluble high-molecular compound.Instantiation comprises: such as the water-soluble polymers of polyvinyl alcohol (PVA), and polyvinylpyrrolidone, acid cellulose, gelatin, gum arabic and polyacrylic acid.Particularly use polyvinyl alcohol (PVA) as key component, aspect the fundamental characteristics of the oxygen barrier and the property removed of developing, obtaining optimum efficiency.The polyvinyl alcohol (PVA) that is used for protective seam can partly be replaced by ester, ether or acetal, as long as polyvinyl alcohol (PVA) comprises and makes it have oxygen barrier character and water-soluble necessary unsubstituted vinyl alcohol units.Polyvinyl alcohol (PVA) can also contain other copolymerization component of part.The example of polyvinyl alcohol (PVA) comprises that degree of hydrolysis is that 71～100 moles of %, weight-average molecular weight are 300～2,400 polyvinyl alcohol (PVA).Instantiation comprises: PVA-105, PVA-110, PVA-117, PVA-117H, PVA-120, PVA-124, PVA-124H, PVA-CS, PVA-CST, PVA-HC, PVA-203, PVA-204, PVA-205, PVA-210, PVA-217, PVA-220, PVA-224, PVA-217EE, PVA-217E, PVA-220E, PVA-224E, PVA-405, PVA-420, PVA-613 and L-8 (all these is by Kuraray Co., and Ltd. makes).The component of protective seam (comprising the selection of PVA and the use of adjuvant), Tu Liang etc. have considered oxygen barrier, the development property removed, mist formation, adhesiveness and mar proof and have selected.Generally speaking, the degree of hydrolysis of used PVA high more (the content of substituted ethylene alcohol unit is not high more in the protective seam) and film thickness are thick more, and be high more to the shielding of small-molecule substance, is favourable aspect sensitivity therefore.But, when the shielding to small-molecule substance extremely increases, can cause following problem, for example when manufacturing and undressed raw material storage unnecessary polyreaction taking place, and produces the unnecessary mist and the overstriking of image line when imaging exposes.Equally and the adhesiveness of image area and mar proof when handling galley, also be very important.That is, when the hydrophilic layer of being made up of water-soluble polymers is laminated on the lipophilicity recording layer, film takes place easily owing to lack adhesion separate, thereby cause defective at separating part, for example the polymerization inhibiting effect owing to oxygen makes film solidify variation.On the contrary, in order to improve this adhesiveness between two-layer, multiple suggestion has been proposed.For example, U.S.P 292,501 and 44,563 are described to: the acrylic acid emulsion of 20～60 weight % or water-soluble polyethylene pyrrolidone-ethene acetal copolymer are mixed into mainly in the hydrophilic polymer of being made up of polyvinyl alcohol (PVA), and mixture layer is pressed on the recording layer, obtain enough adhesivenesses.
For protective seam of the present invention, can use any known technology.The coating process of protective seam is described in detail in, and for example U.S.P 3,458,311 and JP-A-55-49729 in.
(exposure, development and printing)
Using polymerisable compound of the present invention to form in the Lighographic printing plate precursor of recording layer at carrier surface, record carries out with infrared laser. also can carry out hot record with uviol lamp or heat head. among the present invention, preferably use and can be 760nm～1 by radiation wavelength, ultrared solid state laser or the semiconductor laser of 200nm carry out image exposure.
After with the infrared laser exposure, preferred water or alkaline aqueous solution develop to polymerisable compound of the present invention.
When using alkaline aqueous solution, can use developer solution and the additional liquid of known conventional alkaline aqueous solution as polymerisable compound of the present invention as developer solution.The example comprises inorganic alkaline salt, sodium silicate for example, potassium silicate, tertiary sodium phosphate, tripotassium phosphate, triammonium phosphate, sodium hydrogen phosphate, dipotassium hydrogen phosphate, diammonium hydrogen phosphate, sodium carbonate, sal tartari, hartshorn salt, sodium bicarbonate, saleratus, ammonium bicarbonate, sodium borate, potassium borate, ammonium borate, NaOH, ammonium hydroxide, potassium hydroxide and lithium hydroxide.Can also use organic basic reagent, monomethyl amine for example, dimethylamine, trimethylamine, monoethyl amine, diethylamine, triethylamine, Mono Isopropylamine, diisopropylamine, tri-isopropyl amine, n-butylamine, monoethanolamine, diethanolamine, triethanolamine, an isopropanolamine, diisopropanolamine, ethylene imine, ethylene diamine and pyridine.
These alkaline reagents can use separately or two or more are used in combination.
In addition, when developing with automatic processor, known in developer solution, adding a kind of identical with developer solution or alkaline aqueous solution (replenishing liquid) that is higher than developer solution, a large amount of Lighographic printing plate precursors can be made, and the developer solution that uses in the developing trough can be do not changed for a long time.This supplement mode also is preferred use the among the present invention.
For quicken or postpone to develop, the diffusion of development scum silica frost, and increase the parent-oiliness of galley image area, can in developer solution and additional liquid, add kinds of surface activating agent and organic solvent as required.As for surfactant, negative ion, kation, nonionic and amphoteric surfactant are preferred.As for organic solvent, preferred phenmethylol.Also preferably add the polyglycol or derivatives thereof, perhaps the propylene glycol or derivatives thereof.
The sugar that can also add irreducibility, for example arabitol, D-sorbite and mannitol.
In addition, can also add quinhydrones as required in developer solution and additional liquid, resorcinol is such as the inorganic salts base reductant of sodium sulphite or potassium or sodium bisulfite or sylvite, organic carboxyl acid, defoamer, perhaps water softening agent.
The galley of developing with developer solution and additional liquid is carried out aftertreatment, for example use wash-down water, contain the cleaning fluid of surfactant etc., and the quick solution that goes that contains gum arabic or starch derivative carries out aftertreatment.When using polymerisable compound of the present invention, can adopt the various combinations of these processing to carry out aftertreatment as printing plate material.
In plate-making and printing industry,, be extensive use of the robotization processor of printing plate material in recent years in order to realize rationality and standardization.This automatic processor generally comprises develop part and aftertreatment part, also comprise the unit and each processing liquid pool and the injection unit that are used to transmit galley, wherein Bao Guang galley is transmitted by level and is developed, simultaneously with pump pick up each treating fluid by nozzle ejection on version.Recently, also having a kind of known method, is to handle galley in handling liquid pool, handle in the liquid pool to be full for the treatment of fluid, and galley is soaked wherein and by the deflector roll transmission.In this automatic processing, can when handling, in each treating fluid, add additional liquid according to treatment capacity and running time.And, also can come automatic Supplementary Division reason liquid by the sensor conductivity.
Can also adopt so-called non-recycling system, this system is handled with brand-new substantially treating fluid.If desired, can after being coated with up quick natural gum, the lithographic plate that obtains like this carry out print steps again.When requiring lithographic plate to have higher printability resistance, lithographic plate is fired processing.When lithographic plate being fired processing, preferably before firing, use JP-B-61-2518, JP-B-55-28062, the surperficial conditioning liquid described in JP-A-62-31859 and the JP-A-61-159655 is handled lithographic plate.
The method example that carries out this processing comprises following method: with having flooded the sponge of surperficial conditioning liquid or absorbent cotton surperficial conditioning liquid is coated in method on the lithographic plate, be immersed in lithographic plate in the cylinder that surperficial conditioning liquid is housed and be coated with the method for upper surface conditioning liquid, and the method that is coated with the upper surface conditioning liquid with automatic coating machine. can also be after coating, make the amount of being coated with even with squeegee or squeegee, thereby obtain preferred result.
The suitable amount of being coated with of surface conditioning liquid is generally 0.03～0.8g/m 2(with dry weight basis).As required, after being coated with the lithographic plate drying of surperficial conditioning liquid, at high temperature heat this version with burn processing machine (for example FujiPhoto Film Co., the burn processing machine " BP-1300 " that Ltd. sells) etc.At this moment, heating-up temperature and time decide according to the component kind that forms image, preferably heat 1～20 minute under 180～300 ℃ of temperature.
If desired, can be to suitably carry out the conventional processing of adopting, for example washing and gluing through the lithographic plate of firing processing.When what use is when containing the surperficial conditioning liquid of water-soluble high-molecular compound, can omit so-called quick processing, for example gluing of going.
To be fixed on the offset machine through the lithographic plate that obtains from polymerisable compound of the present invention of this processing, produce a large amount of printed matters.
Embodiment
Embodiment
Describe the present invention in more detail with reference to following embodiment below, but be to be understood that the present invention is not limited to these embodiment.Additional disclosure in the application's embodiment, is to using polymerisable compound of the present invention to assess as the lithographic plate of recording materials, polymerisable compound of the present invention being assessed from assessment result again once.
[confirmation that polarity transforms]
The compound (A) and the comparative compound that will be used for the following examples carry out differential thermal analysis (DTA), to determine to take place the temperature (being described as " polarity inversion temperature " in table) of the loss in weight.Then, under this temperature, rely on NMR to discern this pyrolysis compound, to confirm the generation of decarboxylation or dehydrogenation.
The polarity inversion temperature of each compound is shown in the following table 1.
[table 1]
Example compound The polarity inversion temperature (℃)
(4) 227
(43) 200
(41) 137
(25) 180
(28) 198
(35) 201
(46) 210
Example compound The polarity inversion temperature (℃)
(51) 223
(52) 184
(53) 196
(A-1) 205
(A-10) 197
(A-15) 182
H-1 Nonpolarity conversion
H-2 Nonpolarity conversion
H-3 Nonpolarity conversion
[embodiment 1～23 and comparative example 1～2]
(preparation of carrier)
JIS A1050 alloy (containing more than or equal to 99.5% aluminium 0.30%Fe, 0.10%Si, 0.02%Ti and 0.013%Cu) melt is carried out cleaning and casting.In cleaning, in order to remove gas unnecessary in the melt, hydrogen for example, the processing that outgases, and carry out the ceramic pipe filter process.Casing process is the DC casting method.To plate thickness is that the dark from the teeth outwards 10mm place of curing ingot bar of 500mm carries out surface grinding, and the processing 10 hours that homogenizes under 550 ℃ then makes not roughening of intermetallics.
Then, the gained ingot bar is carried out hot rolling under 400 ℃, semi-manufacture 500 ℃ of down annealing 60 seconds, carry out cold rollingly in continuous annealing furnace again, and the aluminium that forms thickness of slab 0.30mm rolls plate.By the roughness of controlled rolling cylinder, the center line average surface roughness (Ra) after cold rolling is controlled in 0.2 μ m.After this, more flat in order to make plate, handle rolling plate with tension level(l)er.
Then, carry out surface treatment, make it become the carrier of lithographic plate rolling plate.
At first,, aluminium sheet is carried out ungrease treatment, handled 30 seconds down at 50 ℃ with 10% sodium aluminate aqueous solution in order to remove the rolling oil of surface of aluminum plate, and with 30% aqueous sulfuric acid 50 ℃ down in 30 seconds, carry out ungrease treatment.Then, the gained aluminium sheet is carried out so-called blasting treatment, improving the adhesiveness between carrier and the recording layer, and make non-image district have water-retaining property.The electrolysis sandblast is performed such: will contain 1% nitric acid and 0.5% aqueous solution of aluminum nitrate and remain on 45 ℃, the aluminium net is imported in the aqueous solution, and apply the waveform alternating current, current density is 20A/dm 2, duty ratio is 1: 1, is 240C/dm from indirect anodization electric weight for battery 2After this, the aluminium sheet that obtains 50 ℃ of following etchings with 10% sodium aluminate aqueous solution 30 seconds, and with 30% aqueous sulfuric acid 50 ℃ down in and 30 seconds, carry out decontamination point processing.
In addition, in order to improve wearing quality, chemical resistance and water-retaining property, on carrier, forming oxide film by anodic oxidation. 20% aqueous sulfuric acid that uses 35 ℃ adopts to supply battery indirectly as electrolytic solution, when the aluminium net enters electrolytic solution, uses 14A/dm 2Direct current the aluminium net is carried out electrolytic treatments, prepare 2.5g/m 2Anode oxide film.
(formation recording layer)
Preparation has the recording layer masking liquid 1 of following composition, be coated with the line rod on the alumina supporter that obtains in the above, in Warm-air dryer in 115 ℃ of dryings 45 seconds, the formation recording layer.The dried amount of being coated with of recording layer that forms is 1.2～1.3g/m 2In addition, coat external coating masking liquid, in Warm-air dryer,, obtain Lighographic printing plate precursor of the present invention in 120 ℃ of dryings 75 seconds with following composition with sliding hopper.The external coating amount of being coated with of Huo Deing is 2.3g/m like this 2
＜recording layer masking liquid 1 〉
Component (A): (monobasic) carboxylic acid (compound and quantity see Table 2)
Component (B): radical initiator (compound sees Table 2) 0.35g
Component (C): polymerisable compound (M-1) (having structure as follows) 2.00g
Component (D): infrared absorbent (IR-1) (having structure as follows) 0.08g
Component (E): binder polymer (compound sees Table 2) 2.0g
The naphthalene sulfonate 0.04g of Victoria's ethereal blue
Fluorine based surfactant (Dainippon Ink and Chemicals, Incorporated makes the Megaface F-176 of 0.01g)
Methyl ethyl ketone 9.0g
Methyl alcohol 10.0g
1-methoxyl-2-propyl alcohol 8.0g
＜external coating masking liquid 〉
Polyvinyl alcohol (PVA) (degree of hydrolysis: 98.5 moles of %, the degree of polymerization: 500) 2.5g
Polyvinylpyrrolidone (Tokyo Kasei Kogyo Co., the K30 that Ltd. makes, molecule 0.5g amount: 40,000)
Non-ionic surfactant (Nihon-Emulsion Co., the EMAREX 0.05gNP-10 that Ltd. makes)
Ion exchange water 96.95g
Additional disclosure once, the compound (A) that the embodiment of the invention is used is to contain the compound of the group of being represented by top illustrational formula (I) or the compound of being represented by top illustrational formula (I-A), the monocarboxylic acid compound (H-1) that uses in the comparative example, (H-2) and (H-3) be carboxylic acid compound beyond the scope of the invention, its structure is as follows.
Figure G2004100070091D00971
What list below is the structure of the radical initiator (S-1)～(S-6) that uses in the embodiment of the invention and the comparative example.
What list below is the structure of the polymerizable compound (M-1)～(M-3) that uses in the embodiment of the invention and the comparative example.
Figure G2004100070091D00991
What list below is the structure of the infrared absorbent (IR-1)～(IR-3) that uses in the embodiment of the invention and the comparative example.
What list below is the structure of the binder polymer (P-1)～(P-3) that uses in the embodiment of the invention and the comparative example.
(exposure)
With Creo ' the s Trendsetter 3244VFS that is furnished with water-cooled 40W infrared semiconductor laser every Lighographic printing plate precursor of gained is exposed, condition is to be output as 9W, and the external drum revolution is 210rpm, and the version surface energy is 100mJ/cm 2, resolution is 2,400dpi.
(development treatment)
After the exposure, use automatic processor, Fuji Photo Film Co., the Stablon 900N that Ltd. makes develops to the Lighographic printing plate precursor of each exposure.As for developer solution, use Fuji Photo Film Co., (1/4) water diluent of the DV-2 that Ltd. makes is both as packing liquid into, again liquid as a supplement.The temperature of developer solution is set to 30 ℃.Also use Fuji Photo Film Co., FN-6 (1/1) water diluent (pH=10.8) that Ltd. makes is as dressing agent.
[printability resistance assessment]
Use Roland ' s R201 printing machine that each lithographic plate of gained is printed, used China ink is Dainippon Ink and Chemicals, GEOS-G (N) China ink that Incorporated makes.Observe the printed article in solid-state image district, the paper number when beginning to fog according to image detects printability resistance.Number is many more, and printability resistance is excellent more.The results are shown in Table 2.
[sensitivity assessment]
Write down necessary energy based on following data computation: by above-mentioned exposure (is the infrared laser exposure of about 830～850nm with wavelength) with the live width of the image that obtains of developing, laser instrument is exported, the loss of optical system and sweep speed.Numerical value is more little, shows that sensitivity is big more.The results are shown in Table 2.
As clearly visible in the table 2, the lithographic plate that has been noted that the embodiment 1～23 that has added The compounds of this invention (A) is compared with the lithographic plate of the comparative example 1～2 that does not add monocarboxylic acid compound of the present invention, and is more excellent aspect printability resistance and sensitivity.
[embodiment 24～39 and comparative example 3～5]
(formation undercoat)
The undercoat masking liquid that will have a following composition with the line rod is coated on the alumina supporter identical with embodiment 1, water wind exsiccator 90 ℃ dry 30 seconds down.The amount of being coated with of the undercoat of Huo Deing is 10mg/m like this 2
＜base coat solution 〉
Beta-alanine 0.1g
Benzene sulfonic acid 0.1g
Methyl alcohol 40g
Pure water 60g
(formation recording layer)
Then, preparation has the recording layer masking liquid 2 of following composition, be coated in the line rod on the alumina supporter of above-mentioned primary coat, in Warm-air dryer in 115 ℃ of dryings 45 seconds, the formation recording layer.The dried amount of being coated with of recording layer that forms is 1.2～1.3g/m 2In addition, coat the external coating masking liquid identical, in Warm-air dryer,, obtain Lighographic printing plate precursor in 120 ℃ of dryings 75 seconds with embodiment 1 with sliding hopper.The external coating amount of being coated with of Huo Deing is 2.3g/m like this 2
＜recording layer masking liquid 2 〉
Component (A): (monobasic) carboxylic acid (compound and quantity see Table 3)
Component (B): radical initiator (S-1) 0.35g
Component (C): polymerisable compound (compound sees Table 3) 2.00g
Component (D): infrared absorbent (IR-1) 0.08g
Component (E): binder polymer (compound sees Table 3) 2.0g
The naphthalene sulfonate 0.04g of Victoria's ethereal blue
Fluorine based surfactant (Dainippon Ink and Chemicals, Incorporated makes the Megaface F-176 of 0.01g)
Methyl ethyl ketone 9.0g
Methyl alcohol 10.0g
1-methoxyl-2-propyl alcohol 8.0g
(exposure and development treatment)
Adopt the mode identical with embodiment 1, to each Lighographic printing plate precursor that obtains like this with the infrared laser exposure and develop the acquisition lithographic plate.
[assessment of the printability resistance in non-image district and anti-staining property and storage stability]
The Lithrone printing machine made from Komori Corporation prints each lithographic plate of gained, and used China ink is Dainippon Ink and Chemicals, DICGEOS-G (N) the Black China ink that Incorporated makes.At this moment, how many range estimations can print and open paper when keeping enough black density, thereby assesses the printability resistance and anti-the staining property in non-image district.
In addition, the Lighographic printing plate precursor that obtains is so forcibly stored 3 days down at 60 ℃ respectively, with under 45 ℃, 75%RH humidity, store 3 days, carry out identical printing operation then, assess the printability resistance and anti-the staining property (storage stability) in non-image district.The results are shown in Table 3.
As clearly visible in the table 3, the lithographic plate that has confirmed to add the embodiment 24～39 of The compounds of this invention (A) is compared with the lithographic plate of the comparative example 3～5 that does not add The compounds of this invention (A), do not form stain in non-image district, and more excellent aspect printability resistance and storage stability.
[embodiment 40～56 and comparative example 6～9]
(formation undercoat)
As follows, the fluid composition (sol solutions) of preparation SG method forms undercoat on the carrier identical with embodiment 1.
＜sol liquid composition 〉
Methyl alcohol 130g
Water 20g
The phosphatase 11 6g of 85% weight
Tetrem oxosilane 50g
3-methacryloxypropyl trimethoxy silane 60g
Mixing is also stirred above-mentioned sol liquid composition.Found that mixing and stirring begin to produce heat after about 5 minutes.After reaction 60 minutes, content is transferred in another container, add 3 then, the methyl alcohol of 000g obtains sol liquid.
(weight ratio: mixture diluted 9/1), and being coated on the carrier identical with embodiment 1 makes the Si amount on the carrier be 30mg/m with methyl alcohol and ethylene glycol with this sol liquid 2, descended dry 1 minute at 100 ℃ subsequently, form undercoat.
(formation recording layer)
Then, the recording layer masking liquid 3 that will have following composition with the line rod is coated on the alumina supporter of above-mentioned primary coat, and in Warm-air dryer in 115 ℃ of dryings 45 seconds, form recording layer.The dried amount of being coated with of recording layer that forms is 1.2～1.3g/m 2In addition, coat the external coating masking liquid identical, in Warm-air dryer,, obtain Lighographic printing plate precursor in 120 ℃ of dryings 75 seconds with embodiment 1 with sliding hopper.The external coating amount of being coated with of Huo Deing is 2.3g/m like this 2
＜recording layer masking liquid 3 〉
Component (A): (monobasic) carboxylic acid (compound and quantity see Table 4)
Component (B): radical initiator (compound sees Table 4) 0.35g
Component (C): polymerisable compound (M-1) 2.00g
Component (D): infrared absorbent (compound sees Table 4) 0.08g
Component (E): binder polymer (P-1) 2.0g
The naphthalene sulfonate 004g of Victoria's ethereal blue
Fluorine based surfactant (Dainippon Ink and Chemicals, Incorporated makes the Megaface F-176 of 0.01g)
Methyl ethyl ketone 9.0g
Methyl alcohol 10.0g
1-methoxyl-2-propyl alcohol 8.0g
(exposure and development treatment)
Adopt the mode identical with embodiment 1, to each Lighographic printing plate precursor that obtains like this with the infrared laser exposure and develop the acquisition lithographic plate.
[assessment of the printability resistance in non-image district and anti-staining property and storage stability]
Adopt the method identical, each lithographic plate of such acquisition is assessed with embodiment 1.
But also adopt the method identical with embodiment 15, and anti-the staining property (storage stability) in each non-image district of Lighographic printing plate precursor of such acquisition is assessed. the results are shown in Table 4.
As clearly visible in the table 4, the lithographic plate that has confirmed to add the embodiment 40～56 of The compounds of this invention (A) is compared with the lithographic plate of the comparative example 6～9 that does not add The compounds of this invention (A), do not form stain in non-image district, and more excellent aspect sensitivity and storage stability.
[embodiment 57～79 and comparative example 10～11]
(formation undercoat)
Handle carrying out silicate with embodiment 1 identical alumina supporter, purpose is to guarantee the water wettability in the non-image district of galley.Processing is performed such: the aluminium net is delivered in 1.5% No. 3 sodium silicate aqueous solutions, contacts 15 seconds, and wash the aluminium net with water.The adhesion amount of Si is 10mg/m 2The Ra of Zhi Bei carrier (center line average surface roughness) is 0.25 μ m like this.
(formation recording layer)
Then, the recording layer masking liquid 4 that will have following composition with the line rod is coated on the alumina supporter of above-mentioned primary coat, and in Warm-air dryer in 115 ℃ of dryings 45 seconds, form recording layer.The dried amount of being coated with of recording layer that forms is 1.2～1.3g/m 2In addition, coat the external coating masking liquid identical, in Warm-air dryer,, obtain Lighographic printing plate precursor in 120 ℃ of dryings 75 seconds with embodiment 1 with sliding hopper.The external coating amount of being coated with of Huo Deing is 2.3g/m like this 2
＜recording layer masking liquid 4 〉
Component (A): (monobasic) carboxylic acid (compound and quantity see Table 5)
Component (B): radical initiator (S-1) 0.40g
Component (C): polymerisable compound (M-1) 1.80g
Component (D): infrared absorbent (IR-1) 0.06g
Component (E): binder polymer (P-1) 2.20g
The naphthalene sulfonate 0.04g of Victoria's ethereal blue
Fluorine based surfactant (Dainippon Ink and Chemicals, Incorporated makes the Megaface F-176 of 0.01g)
Methyl ethyl ketone 9.0g
Methyl alcohol 10.0g
1-methoxyl-2-propyl alcohol 8.0g
(exposure and development treatment)
Each negative planographic printing plate precursor that obtains like this with the infrared laser exposure and carry out development treatment, is obtained lithographic plate.
[assessment of printability resistance and sensitivity]
Adopt the method identical, the printability resistance and the sensitivity of each lithographic plate of such acquisition are assessed with embodiment 1.The results are shown in Table 5.
Table 5
(monobasic) carboxylic acid compound Sensitivity (mJ/cm 2) Printability resistance (number * 10,000)
Embodiment 57 (A-27)0.20g 70 8.5
Embodiment 58 (A-28)0.22g 65 8.3
Embodiment 59 (A-32)0.20g 55 8.5
Embodiment 60 (A-34)0.18g 60 8.2
Embodiment 61 (A-42)0.25g 60 8.6
Embodiment 62 (A-44)0.19g 45 8.4
Embodiment 63 (A-52)0.22g 45 8.4
Embodiment 64 (A-87)0.21g 38 9.3
Embodiment 65 (A-73)0.19g 45 9
Embodiment 66 (A-85)0.19g 36 9.8
Embodiment 67 (A-90)0.21g 38 9.4
Embodiment 68 (A-92)0.19g 37 9.5
Embodiment 69 (A-96)0.21g 37 9.4
Embodiment 70 (A-99)0.20g 36 9.8
Embodiment 71 (A-101)0.22g 36 9.7
Embodiment 72 (28)0.20g 70 8.5
Embodiment 73 (41)0.22g 65 7.9
Embodiment 74 (63)0.20g 55 8
Embodiment 75 (35)0.25g 60 8.6
Embodiment 76 (67)0.19g 45 8.4
Embodiment 77 (33)0.22g 45 8.4
Embodiment 78 (51)0.19g 45 9
(monobasic) carboxylic acid compound Sensitivity (mJ/cm 2) Printability resistance (number * 10,000)
Embodiment 79 (52)0.15g 40 9
Comparative example 10 Do not have 110 4.2
Comparative example 11 (H-1)0.12g 110 3.5
As clearly visible in the table 5, confirmed to add the lithographic plate of the embodiment 57～79 of The compounds of this invention (A)
Galley is compared with the lithographic plate of the comparative example 10～11 that does not add The compounds of this invention (A), and is more excellent aspect printability resistance and sensitivity.
According to top described, clearly: according to the present invention, the polymerisable compound of the present invention that has added the compound (A) of molecular formula (I) representative has excellent sensitivity, printability resistance and storage stability, can be as the image recording material of Lighographic printing plate precursor.
According to the present invention, can obtain can be used as the polymerisable compound of negative planographic printing plate precursor image recording material with excellent sensitivity and storage stability.
The application is based on Japanese patent application JP 2003-43087 that submitted on February 20th, 2003 and the Japanese patent application JP 2003-194852 that submitted on July 10th, 2003, and its full content is incorporated herein by reference document, as setting forth in full.

Claims (2)

1. polymerisable compound, it comprises:
(A-1) a kind of monocarboxylic acid compound by following formula (I-2) expression;
(B) radical initiator;
(C) contain the compound of at least one alkene formula unsaturated link; With
(D) infrared absorbent:
Figure F2004100070091C00011
Wherein:
A represents aromatic radical or heterocyclic radical,
R 1And R 2Represent hydrogen atom separately,
X 1Expression-N (R 3)-and
R 3(ii) represent by following formula:
R wherein 6, R 7And R 8Represent hydrogen atom separately, and Z represents replacement or unsubstituted alkyl or replacement or unsubstituted aryl.
2. Lighographic printing plate precursor, it comprises carrier and recording layer, and described recording layer contains polymerizable compositions according to claim 1.
CN2004100070091A 2003-02-20 2004-02-20 Polymerizable composition and lithographic printing plate precursor Expired - Lifetime CN1525249B (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2003043087 2003-02-20
JP2003043087 2003-02-20
JP2003-043087 2003-02-20
JP2003-194852 2003-07-10
JP2003194852 2003-07-10
JP2003194852A JP4458778B2 (en) 2003-02-20 2003-07-10 Polymerizable composition and planographic printing plate precursor using the same

Publications (2)

Publication Number Publication Date
CN1525249A CN1525249A (en) 2004-09-01
CN1525249B true CN1525249B (en) 2010-05-05

Family

ID=32737741

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2004100070091A Expired - Lifetime CN1525249B (en) 2003-02-20 2004-02-20 Polymerizable composition and lithographic printing plate precursor

Country Status (6)

Country Link
US (1) US7416835B2 (en)
EP (1) EP1449651B1 (en)
JP (1) JP4458778B2 (en)
CN (1) CN1525249B (en)
AT (1) ATE412513T1 (en)
DE (1) DE602004017376D1 (en)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4139724B2 (en) * 2003-04-10 2008-08-27 富士フイルム株式会社 Planographic printing plate precursor
JP2005059446A (en) * 2003-08-15 2005-03-10 Fuji Photo Film Co Ltd Original printing plate for lithographic printing plate and method for lithographic printing
JP4606749B2 (en) * 2004-02-16 2011-01-05 富士フイルム株式会社 Planographic printing method and planographic printing plate precursor used therefor
JP2006160836A (en) 2004-12-03 2006-06-22 Fuji Photo Film Co Ltd Ink for ink jet recording curable by irradiating with radioactive ray and method for making lithographic printing plate using the same
JP4457034B2 (en) * 2005-03-28 2010-04-28 富士フイルム株式会社 Photosensitive planographic printing plate
JP5264082B2 (en) * 2006-08-11 2013-08-14 富士フイルム株式会社 Flexographic printing plate precursor for laser engraving
JP5344790B2 (en) * 2006-12-28 2013-11-20 富士フイルム株式会社 Curable composition, color filter and method for producing the same
US8244057B2 (en) 2007-06-06 2012-08-14 Microsoft Corporation Removal of image artifacts from sensor dust
JP4890388B2 (en) * 2007-08-22 2012-03-07 富士フイルム株式会社 Colored photosensitive composition, color filter and method for producing the same
JP5066471B2 (en) * 2008-03-26 2012-11-07 富士フイルム株式会社 Plate making method of lithographic printing plate precursor
JP5466462B2 (en) * 2008-09-18 2014-04-09 富士フイルム株式会社 Planographic printing plate precursor, method for producing a planographic printing plate, and planographic printing plate
JP2010156881A (en) * 2008-12-29 2010-07-15 Fujifilm Corp Photosensitive composition, colored photosensitive composition, color filter and liquid crystal display
JP2010156879A (en) * 2008-12-29 2010-07-15 Fujifilm Corp Photosensitive composition, color filter and liquid crystal display
JP5541913B2 (en) 2009-12-25 2014-07-09 富士フイルム株式会社 Preparation method of lithographic printing plate
EP2339402A1 (en) 2009-12-28 2011-06-29 Fujifilm Corporation Lithographic printing plate precursor and method of preparing lithographic printing plate
JP5322963B2 (en) 2010-01-29 2013-10-23 富士フイルム株式会社 Planographic printing plate precursor and lithographic printing plate preparation method
JP5346845B2 (en) 2010-02-26 2013-11-20 富士フイルム株式会社 Method for preparing lithographic printing plate and developer for lithographic printing plate precursor
JP5525873B2 (en) 2010-03-15 2014-06-18 富士フイルム株式会社 Preparation method of lithographic printing plate
WO2011125913A1 (en) 2010-03-31 2011-10-13 富士フイルム株式会社 Developer for processing planographic printing plate precursor, method for preparing planographic printing plate using the developer, and method for printing
JP2012073595A (en) 2010-08-31 2012-04-12 Fujifilm Corp Method of manufacturing lithographic printing plate
JP5205505B2 (en) 2010-12-28 2013-06-05 富士フイルム株式会社 Planographic printing plate precursor and its planographic printing method
JP5205483B2 (en) 2011-02-04 2013-06-05 富士フイルム株式会社 Planographic printing plate precursor and plate making method
JP5211187B2 (en) 2011-02-28 2013-06-12 富士フイルム株式会社 Planographic printing plate precursor and plate making method
JP5186574B2 (en) 2011-02-28 2013-04-17 富士フイルム株式会社 Planographic printing plate precursor and plate making method
EP3001249B1 (en) 2011-02-28 2019-12-25 FUJIFILM Corporation Lithographic printing plate precursors and processes for preparing lithographic printing plates
JP5743783B2 (en) 2011-07-27 2015-07-01 富士フイルム株式会社 Photosensitive composition, planographic printing plate precursor, and polyurethane
CN103748518B (en) 2011-08-22 2016-11-23 富士胶片株式会社 Original edition of lithographic printing plate and the method being used for preparing lithographic plate
JP5432960B2 (en) 2011-08-24 2014-03-05 富士フイルム株式会社 Planographic printing plate precursor and lithographic printing plate preparation method
JP5401522B2 (en) 2011-09-15 2014-01-29 富士フイルム株式会社 Coating composition, and image forming material, lithographic printing plate precursor and oxygen-barrier film using the composition
JP5602195B2 (en) 2011-09-27 2014-10-08 富士フイルム株式会社 Planographic printing plate precursor and lithographic printing plate preparation method
JP5740275B2 (en) 2011-09-30 2015-06-24 富士フイルム株式会社 Printing method using on-press development type lithographic printing plate precursor
EP2818930B1 (en) 2012-02-20 2018-08-22 FUJIFILM Corporation Method of concentrating plate-making process waste liquid, and method of recycling plate-making process waste liquid
TWI671343B (en) * 2014-06-27 2019-09-11 日商富士軟片股份有限公司 Thermosetting resin composition, cured film, method for producing cured film, and semiconductor device
US11167375B2 (en) 2018-08-10 2021-11-09 The Research Foundation For The State University Of New York Additive manufacturing processes and additively manufactured products
CN113156765B (en) * 2020-01-07 2022-09-27 北京化工大学 Photoresist composition for ultraviolet nano-imprinting and preparation and application thereof
WO2023032565A1 (en) * 2021-08-30 2023-03-09 富士フイルム株式会社 Photosensitive composition, transfer film, cured film, and pattern formation method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6309792B1 (en) * 2000-02-18 2001-10-30 Kodak Polychrome Graphics Llc IR-sensitive composition and use thereof for the preparation of printing plate precursors
US20020025489A1 (en) * 2000-05-30 2002-02-28 Kazuto Shimada Heat-sensitive composition and planographic printing plate
US20020197564A1 (en) * 2000-10-17 2002-12-26 Hans-Joachim Timpe Stabilized infrared-sensitive polymerizable systems

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4708925A (en) 1984-12-11 1987-11-24 Minnesota Mining And Manufacturing Company Photosolubilizable compositions containing novolac phenolic resin
JP3515846B2 (en) 1995-02-06 2004-04-05 富士写真フイルム株式会社 Negative image recording material
JP4159058B2 (en) 1997-06-13 2008-10-01 コニカミノルタホールディングス株式会社 Image forming material and image forming method
JP2000089455A (en) 1998-09-11 2000-03-31 Mitsubishi Chemicals Corp Photopolymerizable image forming material
DE19906823C2 (en) 1999-02-18 2002-03-14 Kodak Polychrome Graphics Gmbh IR-sensitive composition and its use for the production of printing plates
JP2002082429A (en) 2000-09-08 2002-03-22 Fuji Photo Film Co Ltd Negative type image recording material
JP2002090985A (en) 2000-09-13 2002-03-27 Fuji Photo Film Co Ltd Original plate of planographic printing plate
US6893797B2 (en) * 2001-11-09 2005-05-17 Kodak Polychrome Graphics Llc High speed negative-working thermal printing plates
US6846614B2 (en) 2002-02-04 2005-01-25 Kodak Polychrome Graphics Llc On-press developable IR sensitive printing plates
US20030118939A1 (en) * 2001-11-09 2003-06-26 Kodak Polychrome Graphics, L.L.C. High speed negative working thermal printing plates
US20040091811A1 (en) * 2002-10-30 2004-05-13 Munnelly Heidi M. Hetero-substituted aryl acetic acid co-initiators for IR-sensitive compositions
JP2004012706A (en) * 2002-06-05 2004-01-15 Fuji Photo Film Co Ltd Planographic printing plate original plate
US6899992B2 (en) * 2002-11-08 2005-05-31 Kodak Polychrome Graphics Llc Polymerizable compounds with quadruple hydrogen bond forming groups

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6309792B1 (en) * 2000-02-18 2001-10-30 Kodak Polychrome Graphics Llc IR-sensitive composition and use thereof for the preparation of printing plate precursors
US20020025489A1 (en) * 2000-05-30 2002-02-28 Kazuto Shimada Heat-sensitive composition and planographic printing plate
US20020197564A1 (en) * 2000-10-17 2002-12-26 Hans-Joachim Timpe Stabilized infrared-sensitive polymerizable systems

Also Published As

Publication number Publication date
US7416835B2 (en) 2008-08-26
US20050106495A1 (en) 2005-05-19
EP1449651A3 (en) 2005-05-04
EP1449651A2 (en) 2004-08-25
JP2004310000A (en) 2004-11-04
ATE412513T1 (en) 2008-11-15
DE602004017376D1 (en) 2008-12-11
EP1449651B1 (en) 2008-10-29
CN1525249A (en) 2004-09-01
JP4458778B2 (en) 2010-04-28

Similar Documents

Publication Publication Date Title
CN1525249B (en) Polymerizable composition and lithographic printing plate precursor
CN100503726C (en) Polymerizable composition
CN1664698B (en) Polymerizable composition and lithographic printing plate precursor
JP4393408B2 (en) Negative type planographic printing plate precursor
JP4291638B2 (en) Alkali-soluble polymer and planographic printing plate precursor using the same
CN100590525C (en) Polymerizable composition and plated printed plate fore-body
US7381517B2 (en) Curable composition and image forming material containing the same
JP4090307B2 (en) Preparation method of lithographic printing plate
JP2005263988A (en) Polymerizable composition and image recording material using the same
JP4150261B2 (en) Plate making method of lithographic printing plate precursor
JP4226759B2 (en) Planographic printing plate precursor
JP2005300817A (en) Polymerizable composition and lithographic printing master plate
JP4776899B2 (en) Planographic printing plate precursor
JP2004109851A (en) Resin composition
JP2004302077A (en) Polymerizable composition and lithographic printing original plate using the same
JP4593390B2 (en) Negative image forming material
JP4303534B2 (en) Polymerizable composition
JP2005048143A (en) Polymerizable composition
JP2006091189A (en) Negative image recording material
JP4262945B2 (en) Thermal / photosensitive composition
JP2004302184A (en) Polymerizable composition and lithographic printing original plate using the same
JP2004309897A (en) Polymerizable composition and negative image recording material
JP2004300315A (en) Polymerizable composition
JP4629741B2 (en) Preparation method of lithographic printing plate
JP2003107751A (en) Method for making up original plate for planographic printing plate and planographic printing plate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: FUJI PHOTO FILM CO., LTD.

Free format text: FORMER OWNER: FUJIFILM HOLDINGS CORP.

Effective date: 20070727

C41 Transfer of patent application or patent right or utility model
TA01 Transfer of patent application right

Effective date of registration: 20070727

Address after: Tokyo, Japan

Applicant after: FUJIFILM Corp.

Address before: Tokyo, Japan

Applicant before: Fujifilm Corp.

C14 Grant of patent or utility model
GR01 Patent grant
CX01 Expiry of patent term
CX01 Expiry of patent term

Granted publication date: 20100505